A
Abatacept
for juvenile idiopathic arthritis,
838t
Abbreviations in laboratory testing,
e708-1t
ABCB11 gene defect,
1383t
ABCDE assessment in pediatric emergency,
279
ABCs of resuscitation,
575
Abdomen
eating disorders effects on,
93t
malnutrition effects on,
175t
Abdominal distention,
1249
nondigestive causes of,
1241t
Abdominal epilepsy,
1247t
Abdominal mass(es),
1249
in newborn assessment,
535
nondigestive causes of,
1241t
Abdominal pain,
1247-1248,
1247t-1248t
in acute intermittent porphyrias,
e85-6
in acutely ill child,
276
in
Campylobacter infection,
969
exclusion from day care due to,
e15-2t
in hyperparathyroidism,
1921
nondigestive causes of,
1241t
of peptic ulcer disease,
1292
Abdominal palpation
in acutely ill child evaluation,
276-277
Abdominal tenderness in appendicitis,
1350
Abdominal tuberculosis,
1006
Abdominal undescended testis,
1859
Abdominal visceral nerve block,
372
Abducens nerve
neurologic examination of,
e584-4
Ablation
catheter, for supraventricular tachycardia,
1614-1615
Abscess
epidural, poliovirus infection
versus,
1085t
fever of unknown origin in,
900t
muscle,
Staphylococcus aureus,
905
Absolute bioavailability in drug therapy,
e57-2
Absolute eosinophilia count,
739-740
Absolute neutrophil count (ANC)
in fever of unknown origin,
901
Abstinence-only sex education,
701-702
Abuse and neglect,
135-147
definitions associated with,
135-136
factitious disorder by proxy as,
146-147
foster and kinship care and,
e35-1
in foster care children,
e35-2t
traumatic retinopathy related to,
2180,
2181f
United States situation regarding,
136
ABVD regimen for Hodgkin lymphoma,
1742,
1743t
ABVE-PC regimen for Hodgkin lymphoma,
1742,
1743t
Accelerated junctional ectopic tachycardia (JET),
1615
Acceleration of fetal heart rate,
543-544
Acceptable macronutrient distribution range (AMDR),
e41-1t,
e41-4
Accessory nerve, neurologic examination of,
e584-5
Accountable Care Organizations,
e2-7
Accreditation, child care,
e15-1
Accreditation Council for Graduate Medical Education (ACGME),
e2-3
Accuracy of laboratory tests,
e707-1
Acetabular labrum tear,
2414
Acetaxolamide-responsiveness myotonia,
2125t
Acetazolamide
adverse effects of,
2031t
Acetoacetyl CoA thiolase deficiency (ACAT
2),
433-434
Acetylcholine (ACh), myasthenia gravis and,
2132,
2133t
Acetylcholine (ACh) inhibitors, for myasthenia gravis,
2135t
N-Acetylcysteine for acetaminophen poisoning,
256t-257t,
259
Achondrogenesis type 1B,
2431
Acid-base disorders
terminology associated with,
229-230
Acid-fastness of mycobacteria,
996
Acidosis
cardiac arrest due to,
289t
following open heart surgery,
1604
lactic,
232
in type I glycogen storage disease,
492-493
metabolic,
230t-231t,
231-235
in chronic kidney disease,
1824
clinical manifestations of,
233
as complication of enterocystoplasty,
e536-2
hypophosphatemia and,
227
in respiratory distress syndrome,
586
in tetralogy of Fallot,
1574
Acids
household
conjunctivitis due to,
2168
secretion of in peptic ulcer disease,
1291-1294
Aciduria
3-hydroxy-3-methylglutaric,
435
N-carbamyl-β-amino,
e83-8
Acoustic reflex test (ART),
2195
Acquired immunodeficiency syndrome (AIDS)
See HIV/AIDS
Acrocyanosis in newborn,
533
Acromioclavicular (AC) separation,
2409,
2410f
Acropustulosis, infantile,
2220
Actinobacillus bacteria in periodontitis,
1257
Action signs, mental health,
57,
57t
Activated partial thromboplastin time (APTT),
1697
reference values for,
1698t
Activation-induced cytidine deaminase (AICDA), mutations in,
726-727
Active sleep behavioral state,
e7-2
Activin in testicular function,
e576-4
Activity restriction
due to chronic illness,
e39-1t
Actonitum species toxicity,
269t
Acute chest syndrome (ACS), in sickle cell disease,
1667-1668
Acute generalized exanthematous pustulosis (AGEP),
e637-9f
Acute genital ulcer (AGU),
708,
709t
Acute hemorrhagic edema (AHE),
870
Acute idiopathic pulmonary hemorrhage (AIPH),
1503,
1504f
Acute illness
drowning and submersion injury as,
341-348
mechanical ventilation for,
321-329
neurologic emergencies as,
e63-1-e63-3
hypoxic-ischemic insult and encephalopathy,
301-303
respiratory distress and failure as,
314-333
Acute inflammatory upper airway obstruction,
1445-1450
Acute lymphocytic leukemia (ALL),
1732-1737
differential diagnosis of,
1734
hematopoietic stem cell transplantation for,
757,
758f
incidence and survival rates for,
1726t
secondary, due to radiation therapy,
e699-5t
supportive care for,
1736
Acute otitis media (AOM),
2199-2201
Moraxella catarrhalis in,
e188-1
in parainfluenza viruses,
1125t
Acute promyelocytic leukemia (APL),
1737-1738
Acute renal failure (ARF),
1818-1822,
1818t
clinical manifestations and diagnosis of,
1819
Acute respiratory distress syndrome,
316
Acute respiratory failure
due to congenital central hypoventilation syndrome,
1520-1522
infections associated with,
1525
due to myelomeningocele with Arnold-Chiari type II malformation,
1522
due to neuromuscular diseases,
1520t
due to obesity hypoventilation syndrome,
1522-1523
due to obstructive sleep apnea,
1523
due to spinal cord injury,
1523
Acute tubular necrosis (ATN),
1819
Acyanotic congenital heart disease
absence of pulmonary valve as,
1571
in adults, contraception and,
1609
aorticopulmonary window defect as,
1561
atrial septal defect as,
1551
coronary-cameral fistula as,
1561
mitral valve prolapse as,
1572
partial anomalous pulmonary venous return as,
1553-1554
pulmonary valve stenosis
infundibular and double chamber right ventricle as,
1564
intracardiac shunt with,
1564
pulmonary valvular insufficiency as,
1571
sinus venosus atrial septal defect,
1553
supracristal ventricular septal defect with aortic insufficiency as,
1559
tricuspid regurgitation as,
1572
Acyl CoA dehydrogenase deficiency
Adalimumab
for juvenile idiopathic arthritis,
838t
Adapalene for acne,
2325t
Adductor response, crossed,
e584-7
Adenine phosphoribosyltransferase (APRT) deficiency,
e83-5
Adenoid cystic carcinoma,
1504
Adenoma
prolactin-secreting pituitary,
e554-3
Adenosine
for pediatric resuscitation and arrhythmias,
294t
Adenosine deaminase (ADA) deficiency,
732
Adenosine triphosphate (ATP)
Adenosylcobalamin deficiency,
e448-5
Adenotonsillectomy for obstructive sleep apnea,
51
Adenylosuccinate lyase (ADSL) deficiency,
e83-6
Adherence
diabetes mellitus therapy,
1986
drug therapy,
e57-12
in asthma management,
788
after renal transplantation,
e530-6
Adhesions, intestinal,
1287
Adhesive otitis media,
2212
Adipose tissue, insulin level effects on,
1975t
Adjustment, chronic illness and,
e39-2
Adjuvants in immunizing agents,
883
Adnexal torsion of ovary,
1871
Adolescence, defined,
649
Adolescent
aggressive periodontitis in,
1257
appendicitis diagnosis in female,
1353
atopic dermatitis in,
804
bariatric surgery for,
186
breast development in,
685
disruptive behavioral disturbances in,
99-100
drowning or submersion injury to,
342
growth and development of,
650t
charts for assessment of,
e13-2
during late adolescence,
654
health enhancement for,
667
idiopathic anterior knee pain syndrome in,
2354
injury risk factors for,
20
intellectual disability in,
125
iron deficiency-anemia due to,
1656
leading causes of death for,
5t
pregnancy of,
699-702,
e87-1
characteristic of teen parent in,
700-701
clinical manifestations of,
700
counseling and initial management of,
700
health care for parents and children in,
702t
medical complications of mothers and babies in,
701
psychosocial outcomes/risk for mother and child in,
701-702
recommended immunization schedule for,
889
response of to divorce,
e16-1
response to death by,
e16-4
sexual identity development in,
654-658
factors that influence,
655
gender variance/gender role nonconformity in,
655-656
gender variant identity/transgender children in,
656-658,
657t
sexually transmitted diseases in,
705-714
substance abuse by,
671-685,
671f
motor vehicle accidents and,
22
21 critical health objectives for,
662t,
663
X-linked adrenoleukodystrophy in,
468
Adolescent-limited offenders,
669
Adoption and Safe Families Act,
e35-1
Adrenal androgens
excess of in congenital adrenal hyperplasia,
1933
Adrenal crisis,
1927
treatment of vomiting associated with,
1244t
Adrenal gland
disorders of
primary aldosteronism as,
e572-1
hemorrhage into,
1927
as delivery room emergency,
578
histology and embryology of,
e568-1
X-linked adrenoleukodystrophy and dysfunction,
468
Adrenal hyperplasia
congenital,
1930-1939,
1931f
adrenocortical insufficiency due to,
1924,
1925t
due to 3β-hydroxysteroid dehydrogenase deficiency,
1936
metabolic alkalosis in,
236
Adrenal hypoplasia congenita (AHC),
1924
Adrenal rests, testicular,
e578-1
Adrenarche, premature,
1894
α-Adrenergic agonists
for psychiatric disorders,
63
α-Adrenergic blockers for urinary lithiasis,
770-773
Adrenocorticotropic hormone (ACTH),
e550-2
in Cushing syndrome,
1939
insensitivity syndromes of,
1925t
Adult, gonococcal infection in,
938-939
Adult T-cell leukemia/lymphoma (ATL),
e269-1
Advanced airway management techniques
Advance directive (AD),
e3-2
Adverse drug events (ADEs),
e2-6
Advisory Committee on Immunization Practices (ACIP),
885
Advocacy
in abuse and neglect management,
142
for emergency medical services for children,
e61-5
in intellectual disability management,
129
Aeroallergens,
764
atopic dermatitis and,
806
Aerosolized therapy for cystic fibrosis,
1492
Affordability of health care for adolescents,
663
Afibrinogenemia, congenital,
1704
African American population
home remedies for fever, colic and teething among,
e4-2t
as special needs population,
7
Africanized honeybee, allergic responses to,
807f
Agammaglobulinemia
B cell immunodeficiency screening and,
720
Agar disk diffusion antimicrobial susceptibility testing,
e164-2-e164-3
Age
gestational
eye examination schedule based on,
2175t
percentile curves for weight and length/stature by,
e9-1f-e9-2f
Age factors
in childhood injuries,
20
in chronic diarrhea,
1343t
Ages and Stages Questionnaire-3 (ASQ-3),
41t-43t
Agglutination test
in group A streptococci infection,
918
Aggrecan-related spondyloepiphyseal dysplasias,
2425
Aggregatibacter bacteria in periodontitis,
1257
Agitation
psychopharmacologic management of,
61t
Agonists, receptor binding by,
e57-8
Aicardi-Goutieres syndrome,
2060t
Air-conduction signals in audiometry,
2193
Air crescent in aspergillosis,
1060
Air embolism, pulmonary,
597
Airway
artificial
for respiratory distress and failure,
319
disorders of in mucopolysaccharidoses,
515t
extrathoracic-extrapulmonary,
e365-5
in pediatric emergency assessment,
279-281
respiratory acidosis due to disease of,
239t
Airway clearance treatment
for respiratory insufficiency,
1525
Airway hyperresponsiveness (AHR),
780
Airway obstruction
critical high airway obstruction syndrome (CHAOS),
577,
578f
respiratory distress due to,
315t
in respiratory syncytial virus infection,
1127-1128
due to tonsil and adenoid pathology,
1443,
1445
Airway pressure release ventilation (APRV),
326
AKR1D1 gene defect,
1383t
Alanine aminotransferase (ALT)
in autoimmune hepatitis,
1409
Alaska Native population, death rates for,
3t-4t
Albright hereditary osteodystrophy,
1919-1920
Albumin
infusion for burn injury,
353
in malnutrition with chronic diarrhea,
1343t
for nephrotic syndrome,
1805
Alcohol
neonatal withdrawal from,
624
porphyria cutanea tarda and,
e85-11
Alcoholism, hypophosphatemia due to,
228
Alcohol use
drowning or submersion injury associated with,
342
maternal
as sudden infant death syndrome risk factor,
1424
Alcohol Use Disorders Identification Test (AUDIT),
678-679,
678t
Aldosterone,
e568-6
deficiency of in congenital adrenal hyperplasia,
1931-1933
synthase deficiency,
1938
Aldosteronism
glucocorticoid-remediable,
236
Alert, Verbal, Pain, Unresponsive (AVPU) Pediatric Response Scale,
281
α-Linolenic acid (ALA),
e41-15
Alkaline phosphatase
rickets due to deficiency of,
e694-2t
Alkalinization, urinary, for poisoning,
258,
260
Alkalis, household
conjunctivitis due to,
2168
Alkalosis,
229-230
forced, for persistent pulmonary hypertension of the newborn,
593
hypochloremic in cystic fibrosis,
1487
Allelic heterogeneity,
e77-2
Allergen immunotherapy
for atopic dermatitis,
805
Allergic bronchopulmonary aspergillosis (ABPA),
1474
immunoglobulin E levels in,
766
Allergic contact dermatitis,
2251
Allergic granulomatosis,
868t
Allergy
acute laryngeal swelling due to,
1448
contact, involving eyes,
810
latex, neuropathic bladder and,
e536-3
Allgrove syndrome,
1264
autonomic neuropathy with,
2142
Allium cepa for asthma,
271t
Allogenic stem cell transplantation,
757,
758t
from HLA-identical sibling,
757-760
Allograft in intestinal transplantation,
e331-2
Alloimmune neonatal neutropenia,
749-750
Alloimmune thrombocytopenic purpura, neonatal,
1720
Alloiococcus otitidis,
2201
All-terrain vehicle (ATV) accident,
22
Almotriptan for migraine,
2044t
Alopecia
disorders associated with,
2289t
α-Adrenergic agents
for attention deficit/hyperactivity disorder,
111t
for psychiatric disorders,
63
for psychosis and agitation,
64t
for systemic hypertension,
1645t
α-Fetoprotein concentration,
543t
in germ cell tumors,
1770
in ovarian carcinomas,
1872t
Alpha-linolenic acid (ALA),
e41-15
Alternating attention,
e29-3
Alveolar alveolitis,
Aspergillus in,
1059
Alveolar-arterial oxygen (A-ao
2) gradient,
318,
e365-8
Alveolar compartment, pulmonary edema and,
1468
Alveolar gas composition,
316
Alveolar hypoventilation,
1523
Alveolar partial pressure of carbon dioxide (PaCO
2),
e365-8
in bronchopulmonary dysplasia,
1521
Alveolar partial pressure of oxygen (Pao
2),
1419,
e365-7
in congenital heart disease evaluation,
1573
Alveolar rhabdomyosarcoma,
1760
Alveolar soft part sarcoma,
1762t
Alveolitis,
Aspergillus in,
1059
Alzheimer’s disease, familial,
e270-2
Ambulance, ground
versus air,
e61-8
Ambulatory blood pressure monitoring (ABPM),
1639-1640
American Academy of Pediatrics (AAP),
12
on complementary feeding,
164
model for quality improvement from,
e2-7
American Association on Intellectual and Developmental Disabilities (AAIDD),
122-124
American Board of Pediatrics (ABP),
12
American College of Medical Genetics, on neonatal screening,
e707-3,
e707-3t
American Heart Association (AHA)
American nightshade, potential toxicity of,
272t-273t
Ametropic amblyopia,
2152
Amino acids
indispensable, dispensable, and conditionally dispensable,
e41-4t
Amino acid metabolism defects,
418-456
malabsorption due to,
1318
odors associated with,
418t
of valine, leucine, isoleucine, and related organic acidemias,
430-438,
430f
α-Aminoadipic semialdehyde dehydrogenase deficiency,
453-454
γ-Aminobutyric acid (GABA)
in status epilepticus,
2038
Aminoglycoside-modifying agents,
e173-1t
5-Amino-4-imidazolecarboxamide (AICA) riboside deficiency,
e83-6
δ-Aminolevulinic acid dehydratase (ALAD) deficiency,
e85-4
δ-Aminolevulinic acid dehydratase porphyria (ADP),
e85-1t,
e85-4
Aminophylline for neonatal apnea,
581
5-Aminosalicylate (5-ASA) for inflammatory bowel disease,
1298-1299
Amiodarone
hypothyroidism due to,
1901
for pediatric resuscitation and arrhythmias,
294t
Amitriptyline
for functional abdominal pain,
1348t
for pain management,
364t
for vomiting prophylaxis,
1244t
Amnesia
as goal of anesthesia,
e70-1
due to shellfish poisoning,
e703-5
Amniotic fluid
in biophysical profile,
543t
diagnostic testing of,
548
Amoxicillin,
e173-4t-e173-11t
for cystic fibrosis lung infection,
1492t
for group A streptococci infection,
918
for
Helicobacter pylori gastritis,
1293t
for infective endocarditis prophylaxis,
1626t
for vulvovaginitis,
1868t
Amphetamine combination for attention deficit/hyperactivity disorder,
62t
Amphetamine salts, mixed for attention deficit/hyperactivity disorder,
111t
Amphotericin B,
e225-1,
e225-1t
for coccidioidomycosis,
1067
possible adverse reactions to in premature infant,
563t
Amphotericin B colloid dispersion (ABCD),
1053,
e225-1t
Amphotericin B deoxycholate
for coccidioidomycosis,
1067
Ampicillin,
e173-4t-e173-11t
for bacterial meningitis,
2093t
for group B streptococci,
927
for infectious diarrhea,
1337t
for meningococcal disease,
933t
for neonatal infection,
645t
for
Salmonella gastroenteritis,
953t
for
Shigella infection,
961
for
Staphylococcus aureus,
907t
Amplitude integrated electroencephalography (aEEG),
571t
Amrinone for heart failure,
e436-5t
Amylin adjunct therapy for type 1 diabetes mellitus,
1979
Amyl nitrate, as inhalant,
681t
Amylo-1,6-glucosidase deficiency,
528
Amyopathic juvenile dermatomyositis,
848
Anaerobic bacterial infections
Clostridium difficile infection as,
994-995
Anakinra
for juvenile idiopathic arthritis,
838t
Anal canal, anatomy of,
1360f
Analgesia/analgesics
See also Pain management
acetaminophen, aspirin, and nonsteroidal antiinflammatory drugs as,
363-364,
364t
for cyclic vomiting syndrome,
1244t
in general anesthesia,
e70-1
pharmacokinetics and pharmacodynamics of,
362-363
in rapid sequence intubation,
287t
in serotonin syndrome,
265t
Anaphylactoid reaction,
816
Anaplastic astrocytoma,
1750
Andersen-Tawil syndrome,
2130
Androgenic drugs, administration during pregnancy,
1962-1963
Androgenic lesion of ovary,
1958
Androgen insensitivity in amenorrhea,
687t
Androgen insensitivity syndromes (AISs),
1966,
1966f
Androgens, adrenal
excess of in congenital adrenal hyperplasia,
1933
Anemia of chronic disease (ACD),
e445-1
Anemia(s),
1648-1650,
1648t
of acute renal failure,
1821
cardiac arrest due to,
289t
chronic hemolysis as,
1653
congenital
Pearson’s syndrome as,
1652
hemolytic
abnormal hemoglobins causing cyanosis as,
1672
abnormal hemoglobins with increased oxygen affinity as,
1671
due to bartonellosis,
982
enteric infection and,
1333t
after Epstein-Barr virus infection,
1114
due to extracellular factors,
e459-1
hereditary elliptocytosis as,
e453-1
hereditary stomatocytosis as,
e454-1
parvovirus B19 infection and,
1095
syndromes of hereditary persistence of fetal hemoglobin as,
1673-1674
history and physical examination in,
1648-1649
laboratory studies in,
1649
parvovirus B19 infection in red cell aplasia as,
1652-1653
renal transplantation and,
e530-2
respiratory signs and symptoms of,
e413-1t
Anesthesia,
359
local
toxicity, neonatal seizures due to,
2034,
2036
Angiocardiography,
1548
in atrioventricular defect,
1555
Angiofibroma, juvenile nasopharyngeal,
1432-1433
Angiography
in liver dysfunction,
1379
magnetic resonance
in attention deficit/hyperactivity disorder,
e30-1
computer processing of,
1546
in orthopedic problems,
2335
in septic arthritis,
2400
Angiokeratoma
in GM
1 gangliosidosis,
483
Angioma
spider, as manifestation of liver disease,
1376
Angioplasty, balloon,
1569
Angiotensin-converting enzyme (ACE),
861
Angiotensin-converting enzyme inhibitors (ACEIs)
for hypertension
of chronic kidney disease,
1825
for Marfan syndrome,
2445
Angiotensin II receptor blockers (ARBs)
for systemic hypertension,
1645t
Angiotensin in aldosterone regulation,
1923
Anicteric leptospirosis,
1024
Animal antisera preparations,
882-883
Animal-born infection
hemorrhagic fevers,
1150t
Rocky Mountain spotted fever,
1041
Animal filariae infection,
1226
Anion gap,
234f
in hyperkalemic renal tubular acidosis,
1811
Anisometropic amblyopia,
2152
Ankle jerk in neurologic examination,
e584-7
Ankle sprain,
2418
in basketball and volleyball,
e684-2
Ann Arbor Conference staging of Hodgkin lymphoma,
1741,
1741t
Anorchia, congenital,
1944
Anorectal disorders,
1355-1362
pilonidal sinus and abscess as,
1362
rectal mucosal prolapse as,
1361
Anorectal manometry (ARM)
in congenital intestinal pseudo-obstruction,
1283t
in Hirschsprung disease,
1286
Anorectoplasty, posterior sagittal,
1358
Anovulatory menstrual cycle,
653
Anoxia, due to drowning,
343
Antacids
for gastroesophageal reflux disease,
1268
hypophosphatemia and,
227
Antagonists, receptor binding by,
e57-8
Antegrade continence enema procedure (ACE),
1359
Antegrade pressure-perfusion flow study,
1841
Antegrade pyelogram,
1841
Anterior cruciate ligament (ACL) injuries,
2414,
2414t
Anterior dislocation of shoulder,
2410
Anterior drawer test,
2415f
Anterior knee pain syndrome,
2354
Anterior lenticonus,
2172
Anterolateral tibial bowing,
2351
Anteromedial tibial bowing,
2351
Anthracycline use, sports participation and,
2402t-2404t
Anthropometric evaluation,
1343
Anti-acetylcholine (ACh) antibodies,
2134
Antiadrenal cytoplasmic antibodies,
1926
Antiandrogens
for familial male gonadotropin-independent precocious puberty,
1893
for polycystic ovary syndrome,
e546-3
Antibiotic-associated diarrhea,
994-995
Antibiotics/antibiotic therapy,
e173-1-e173-14,
e173-4t-e173-11tSee also specific types
child-care setting and,
e167-2
for fever in neutropenic patient,
e171-1
for fever without localizing signs,
898
for group A streptococci infection,
918
for immunocompromised and hospitalized patients,
e173-2
for septic arthritis,
2400
in serotonin syndrome,
265t
for
Shigella infection,
961
for
Staphylococcus aureus infection,
906-908
streptogramins and oxazolidinones in,
e173-14
for vulvovaginal infections,
1868t
Antibodies
autoimmune hemolytic anemia associated with
Antibodies to infliximab (ATI),
1303
Antibody deficiency(ies),
721t,
722-728,
724f
enteroviral meningoencephalitis with,
1092
hyper-immunoglobulin M syndrome as,
726-727
immunoglobulin A deficiency as,
725
immunoglobulin G subclass deficiencies as,
725-726
immunoglobulin heavy- and light-chain deletions as,
726
X-linked lymphoproliferative disease as,
727
Antibody-dependent cellular cytotoxicity (ADCC),
e117-5
Antibody testing
in varicella-zoster virus infection,
1108
Anticholinergic agents
for allergic disease,
770
for motion sickness,
1244t
Anticipatory guidance
for foster care children,
e35-2t
in healthy eating habits,
188t
in injury prevention,
19t
Antidepressants
for migraine prophylaxis,
2044t
for neuropathic pain,
368t
in serotonin syndrome,
265t
tricyclic
for attention deficit/hyperactivity disorder,
111t
for depression and anxiety symptoms,
63t
for neuropathic pain,
368t
in psychopharmacology,
62
Anti-D gamma globulin,
615
Antidiuresis, nephrogenic syndrome of inappropriate,
1884
Antidiuretic hormone (ADH),
e550-2
for central diabetes insipidus,
1883
maintenance fluids and hyponatremia and,
243-244
in osmolality regulation,
e52-4
for portal hypertension,
e359-2
Antiemetics
for nausea and vomiting with migraine,
2043
in serotonin syndrome,
265t
Antiepileptic drugs (AEDs)
for neuropathic pain,
368t
in serotonin syndrome,
265t
Antigen detection
in bacterial and fungal infection diagnosis,
e164-1
in coccidioidomycosis,
1066
in group A streptococci infection,
917-918
in parainfluenza viruses,
1125t
Anti-glomerular basement membrane disease,
e502-3
Antihemophilic factor,
1696t
Antihistamines
for atopic dermatitis,
805
for cyclic vomiting syndrome,
1244t
for migraine prophylaxis,
2044t
for motion sickness,
1244t
Anti-immunoglobulin E
for allergic disease,
772
for atopic dermatitis,
805
Antiinflammatory cytokines,
e117-3t
Antiinflammatory therapy
for cystic fibrosis,
1493
Anti-interleukin-4 drugs,
773
Anti-interleukin-5 drugs,
773
Antimalarial toxicity,
251t
Antimetabolites for atopic dermatitis,
805
Antimicrobial agents
for fever in neutropenic patient,
e171-1
in immunizing agents,
883
Antimicrobial resistance,
e173-1,
e173-1t
child care setting and,
e167-2
Haemophilus influenzae,
941
in neonatal infection,
644
Pseudomonas aeruginosa,
977
Streptococcus pneumoniae,
913
Antimicrobial susceptibility testing,
e164-3
Antimotility agents
for infectious diarrhea,
1337
for traveler’s diarrhea,
e168-5
Antineutrophil cytoplasmic antibody (ANCA)
in inflammatory bowel disease,
1295
in pulmonary hemosiderosis,
1499
Antinuclear antibodies (ANAs)
in juvenile idiopathic arthritis,
836
in systemic lupus erythematosus,
844
Antiphospholipid antibody syndrome (APS),
1709
Antiplasmin
reference values for,
1698t
Antiretroviral therapy, highly active,
1159
Antiseptic skin care of newborn,
537
Antisera preparations,
882t
Antistreptolysin O assay,
918
Antithrombin-III, reference values for,
1698t
Antithrombotic agents,
1710t
Antithymocyte globulin (ATG),
1692
Antithymocyte globulin (ATGAM),
e530-3
α-Antitrypsin
deficiency of,
1393
subcutaneous tissue disease due to,
2283-2284
measurement of
in chronic diarrhea,
1344t
in protein losing enteropathy,
1307
Antroduodenal manometry (ADM),
1283t
Anus
candidal infection of,
2314
newborn assessment of,
536
Anxiety
psychopharmacologic management of,
61t,
63t
respiratory signs and symptoms of,
e413-1t
in type 1 diabetes mellitus,
1986
Anxiety attack, seizure
versus,
e587-4
Anxiety disorders,
77-82,
78t-82t
attention deficit/hyperactivity disorder
versus,
110
Anxiolytic agents,
62
for cyclic vomiting syndrome,
1244t
for depression and anxiety symptoms,
63t
Aortic aneurysm in Marfan syndrome,
2441
Aortic insufficiency,
1628
Aorticopulmonary (AP) window defect,
1561
Aortic stenosis
sudden death due to,
1619
Aortic valve
coarctation with disease of,
1570
Apical pulse, assessment of,
1533
Aplasia
of parathyroid gland,
1917
Aplastic crisis
with transient erythroblastopenia of childhood,
1653
Apley compression test,
2415f
Apnea
congenital myasthenic syndrome with episodic,
2133,
2133t
as delivery room emergency,
575
in factitious disorder by proxy,
146
due to gastroesophageal reflux disease,
1269-1270
sleep
with type 2 diabetes mellitus,
1993t
sudden death syndrome and,
581
Apolipoprotein A-1 (APOA-1) deficiency,
477
Apolipoprotein L-1 (APOL1),
1191
Apophysis
age of appearance and fusion of,
2413t
sports injuries involving,
2408
Apparent life-threatening event (ALTE),
1428
Apparent volume of distribution,
e57-3
Appendageal structures of skin,
e636-1
Appendicitis,
1349-1355
Angiostrongylus costaricensis versus,
1227
physical examination in,
1350
Appetite, control of,
183f
Appetite suppressants, cardiac manifestations of,
1531t
Apple juice, diarrhea and,
1335t
Applied behavior analysis (ABA),
e6-4
Aquatic-borne illness
Plesiomonas shigelloides,
e196-3
Arachidonic acid (ARA),
e41-15
deficiency, cutaneous manifestations of,
2329
Arbovirus in viral meningoencephalitis,
2095-2096
Area under the curve (AUC),
e57-2
Arginine:glycine amidinotransferase (AGAT) deficiency,
441
Argininosuccinate lyase (AL) deficiency,
448f,
452
Argininosuccinate synthetase (AS) deficiency,
451-452
Arnold-Chiari malformations,
1264
myelomeningocele with,
1522
respiratory insufficiency due to,
1522
Aromatase deficiency,
1962
Aromatic amino acid decarboxylase (AADC) deficiency,
445-446,
2060t
Arousal disorders, non-REM partial,
e587-5
Arpiprazole
for mood stabilization,
64t
for psychosis and agitation,
64t
Artemisia absinthium, potential toxicity of,
272t-273t
Arterial baroceptors in respiration regulation,
1421
Arterial dissection,
2080
Arterial ecchymotic Ehlers-Danlos syndrome,
2278
Arterial oxygen content (Cao
2),
e365-8
Arterial partial pressure of carbon dioxide (PaCO
2),
1419,
e365-7-e365-8
peripheral chemoreceptors stimulation and,
1421
Arterial switch procedure
Arteriography, pulmonary,
e366-3
Arteriovenous malformations (AVMs),
2225,
2226f
Arteritis
mesenteric, postoperative,
1569
Arthralgia
in acute rheumatic fever,
922
with parvovirus B19 infection,
1095
Arthritis
See also Rheumatic disease
following meningococcal disease,
933
juvenile idiopathic,
829-839
cardiac manifestations of,
1532t
differential diagnosis of,
835,
836t
fever of unknown origin in,
899
due to parvovirus B19,
1095
suppurative,
Haemophilus influenzae in,
942
Arthrochalasis multiplex congenita,
2278
Arthrogryposis multiplex congenita (AMC),
2387,
e674-1f
Arthropathy, human T-lymphocyte-associated,
e269-1
Arthropod vectors in trypanosomiasis,
1194f,
1195
Arthroscopic surgery for discoid lateral meniscus,
2352,
2352f
Artificial airway
for respiratory distress and failure,
319
Artificial sweeteners,
1982
Arylamine
N-acetyltransferases, drug biotransformation and,
e56-8
Ascending undescended testis,
1859
Ascorbic acid,
194t,
198
dietary needs and sources of,
198
Ashkenazi Jews
persistent hyperinsulinemic hypoglycemia of infancy in,
523
Aspartate aminotransferase (AST)
Aspergilloma, pulmonary,
1059
Aspergillosis, allergic bronchopulmonary,
1474
immunoglobulin E levels in,
766
Aspergillus,
1058-1062
allergic disease due to,
1058
after hematopoietic stem cell transplantation,
762-763
Asphyxia
multiorgan systemic effects of,
569t
Asphyxiating thoracic dystrophy,
1517,
2434
Aspiration,
1469-1471
diagnostic tests of,
1472t
duodenal, in exocrine pancreatic function,
1307
of gastric contents,
1470
joint, in septic arthritis,
2399
pulmonary, in drowning,
343
splenic, in leishmaniasis,
1189
Aspiration pneumonia
due to hydrocarbon toxicity,
267
Aspirin (ASA)
for acute rheumatic fever,
923
gastric ulcer due to,
1293
Asplenia
congenital heart disease with,
1531t
fever without a focus in,
896t
Assassin bugs in trypanosomiasis,
1195
Assist-control (AC) mode in mechanical ventilation,
324
Association studies, genetic,
e77-2
Astatic epilepsy, myoclonic,
2024
Asthma,
780-801
allergen immunotherapy for,
774-775
Aspergillus as trigger of,
1059
clinical manifestations and diagnosis of,
782-783,
784t
differential diagnosis of,
783,
785t
environmental factors in,
781
gastroesophageal reflux disease with,
1269-1270
physical examination in,
765
respiratory syncytial virus infection and,
1129
risk factors for morbidity and mortality associated with,
799t
treatment of,
785-801,
788f
adherence to regimen in,
788
anticholinergic agents for,
796
anti-immunoglobulin E (Omalizumab) for,
796
delivery devices and inhalation techniques for,
796-798
in infants and young children,
800-801
leukotriene-modifying agents for,
795-796
nonsteroidal antiinflammatory drugs for,
796
principles of pharmacology for,
791-793
referral to specialist for,
793
Asymptomatic bacteriuria,
1830
Ataxia,
2054t,
2055
cerebellar
varicella-zoster virus in,
1109
in neurologic examination,
e584-7
strokelike events
versus,
2086
Ataxia-telangiectasia,
735,
2055,
2057t
cutaneous manifestations of,
2230
ovarian defects with,
1956
Ataxia with isolated vitamin E deficiency (AVED),
e49-1
Atelosteogenesis type II,
2431
Atenolol
for systemic hypertension,
1645t
Atlantoaxial anomalies,
2381
Atlantoaxial instability, sports participation and,
2402t-2404t
Atopic dermatitis (AD),
801-807
of external ear canal,
2199
laboratory findings in,
803
Atopic keratoconjunctivitis,
810
ATP8b1 gene defect,
1383t
Atrial ectopic tachycardia,
1615
Atrial natriuretic peptide (ANP),
1527,
1882
Atrial septal defect (ASD),
1551
Atrial septostomy, Rashkind balloon,
1586,
1586f
Atrioventricular (AV) canal defects,
1554-1556
embryonic development of,
1527
Atrioventricular (AV) valves, defects in Marfan syndrome,
2440-2441
Atrioventricular node reentry tachycardia (AVNRT),
1613-1615
Atrioventricular reciprocating tachycardia (AVRT),
1613
Atrium
embryonic development of,
1527
enlargement, electrocardiography of,
1539,
1539f
in fetal circulation,
1529
Atrophy
assessment in neurologic examination,
e584-6
Atropine
for cholinesterase-inhibiting insecticides poisoning,
256t-257t,
267
for pediatric resuscitation and arrhythmias,
294t
in rapid sequence intubation,
287t
Attack, dog-related,
2454
Attention deficit/hyperactivity disorder (ADHD),
108
clinical manifestations of,
108-109
neurodevelopmental function and,
e29-3
sudden death and medications for,
1621
Atypical absence seizure,
2023
Atypical antidepressant toxicity,
265
Atypical squamous cells of undetermined significance (ASCUS),
1139-1140
Atypical teratoid/rhabdoid tumor,
1752
Auditory brainstem response (ABR),
2192,
2195
Auditory canal
congenital stenosis or atresia of,
e630-1
Auditory processing disorders,
2188
Auscultation
of heart sounds
in acutely ill child evaluation,
276
in cardiac examination,
1533
of lungs
in acutely ill child evaluation,
276
Authoritative aspect of eating disorder treatment,
93
Authority gradients for patient safety,
e2-6
Autistic disorder (AD),
100-106,
101t
differential diagnosis of,
101
intellectual disability
versus,
126
Autoantibodies
diabetes mellitus and,
1974
in systemic lupus erythematosus,
842-843
Autoimmune adrenalitis,
1925t
Autoimmune disorders
pulmonary manifestations of,
e413-1t
Autoimmune hypoparathyroidism,
1918
Autoimmune neuropsychiatric disorders associated with
Streptococcus pyogenes,
81,
919
movement disorders associated with,
76
Autoimmune neutropenia,
750
Autoimmune neutropenia of infancy (ANI),
750
Autoimmune ovarian failure,
1956
Autoimmune pancreatitis,
1373
Autoimmune polyendocrinopathy, type I (APS-1),
1926
autoimmune thyroiditis with,
1904
Autoimmune polyendocrinopathy (APS),
1925t,
1969
Autoimmune polyendocrinopathy-candidiasis ectodermal dysplasia (APECED),
730
Autoimmune polyendocrinopathy type II (APS-2),
1926-1927
Autoimmune regulator gene (AIRE),
1409
Autoimmune thrombocytopenic purpura,
1714-1718
Autoimmune thyroiditis,
1903-1905
hypothyroidism due to,
1901
with Turner syndrome,
1953
Autoinflammatory syndrome, familial cold,
855t,
858
Autologous skin test (ASST),
813
Automated external defibrillation (AEDs),
1621
Automatisms in seizures,
2021
Autonomic instability,
e7-2
Autonomic nervous system (ANS)
congenital central hypoventilation syndrome and dysfunction of,
1521
mushroom poisoning effects on,
e703-1
Neonatal Intensive Care Unit Neurobehavioral Scale and,
624t
Auto-positive end-expiratory pressure (PEEP),
328-329
Autoresuscitation, sudden infant death syndrome and,
1428
Autosomal dominant hearing loss,
2189
Autosomal dominant hypoparathyroidism,
1917-1918
Autosomal dominant hypophosphatemic rickets (ADHR),
202t,
207
Autosomal dominant polycystic liver disease (ADPLD),
e357-2
congenital heart disease with,
1531t
Autosomal dominant recurrent fever,
858
Autosomal liver and muscle phosphorylase kinase deficiency,
498
Autosomal liver phosphorylase kinase deficiency,
498
Autosomal recessive dopa-responsive dystonia,
445
Autosomal recessive hearing loss,
2189
Autosomal recessive hypercholesterolemia (ARH),
473t,
475
Autosomal recessive hyper-immunoglobulin M syndrome,
726-727
Autosomal recessive hypoparathyroidism with dysmorphic features,
1917
Autosomal recessive hypophosphatemic rickets (ARHR),
202t
Autosomal recessive proximal renal tubular acidosis,
1808
Autosomal recessive severe combined immunodeficiency,
732-733
Autumn crocus toxicity,
269t
Availability in food security,
170-171
Avian-born infection
Cryptococcus neoformans,
1056
Avidity test in toxoplasmosis,
1214
Awareness during general anesthesia,
e70-11
Axenfeld-Rieger syndrome,
408t
Axillary hair development,
e555-1
Axonal peroneal muscular atrophy,
2139
Azathioprine
for atopic dermatitis,
805
for autoimmune hepatitis,
1410
for lupus nephritis,
1788
Azelastine
for allergic conjunctivitis,
811t
for allergic disease,
771
Azithromycin,
e173-3,
e173-4t-e173-11t
for cat-scratch disease,
985
for
Chlamydophila pneumoniae,
1035
for
Cryptosporidium,
1184
for cystic fibrosis lung infection,
1492t
for infectious diarrhea,
1337t
for
Legionella infection,
e200-2
for Mediterranean spotted fever,
1044
for nongonococcal urethritis,
1033
for nontuberculous mycobacterial prophylaxis,
1015-1016
for sexually transmitted infections in adolescents,
712t
for
Shigella infection,
961
for traveler’s diarrhea,
e168-5
B
Baby foods, nutritive value of,
e708-15t
Bacillary dysentery,
Shigella,
959-961
Bacille Calmette-Guérin (BCG) vaccine,
884t
tuberculin skin testing and,
1001
Back blows for airway obstruction,
282,
283f
Back to Sleep campaign,
1429
Baclofen
for muscle spasm in palliative care,
155t-156t
Bacteremia
due to coagulase-negative staphylococci,
909-910
Haemophilus influenzae,
943
Pseudomonas aeruginosa,
975
Staphylococcus aureus,
905
Staphylococcus epidermis,
910
Bacteria
rapid antigen detection of,
e164-1
Bacterial colonization in neonate,
630
Bacterial infections
anaerobic
Clostridium difficile infection as,
994-995
congenital heart disease and,
1603
fever of unknown origin in,
900t
following organ transplantation,
e171-8
gram-negative
due to
Haemophilus influenzae,
940-943
due to
Neisseria gonorrhoeae,
935-940
due to
Neisseria meningitidis,
929-935
due to
Pseudomonas aeruginosa,
975-977
gram-positive
due to group A streptococcus,
914-925
due to group B streptococcus,
925-928
due to non-group A or B streptococci,
e178-1
due to
Streptococcus pneumoniae,
910-914
predisposition to due to immunodeficiency,
716t
respiratory syncytial virus infection with,
1128
secondary to varicella-zoster virus,
1109
stem cell transplantation and,
e171-1
traveler’s diarrhea due to,
1338t
Bacterial meningitis,
2087-2095
cerebrospinal fluid findings in,
2088t
clinical manifestations of,
2090
Haemophilus influenzae type b in,
2089
pathology and pathophysiology of,
2089
Streptococcus pneumoniae in,
2087
Bacterial resistance,
e173-1,
e173-1t
child care setting and,
e167-2
Haemophilus influenzae,
941
in neonatal infection,
644
Pseudomonas aeruginosa,
977
Streptococcus pneumoniae,
913
Bacterial vaginosis
prophylaxis following rape,
704t
Bacteriuria, asymptomatic,
1830
Baere-Stevenson syndrome,
2012t
Bailler-Gerold syndrome,
2012t
Bald-faced hornet, allergic responses to,
807f
Ballard scoring system,
557
Balloon angioplasty,
1569
Balloon atrial septostomy, Rashkind,
1586,
1586f
Balloon valvuloplasty
for aortic stenosis,
1566
for pulmonary valve stenosis,
1563
Bannayan-Ruvalcaba-Riley syndrome,
e554-2t
Barbiturates
adverse effects of,
2031t
urine screening in adolescent use of,
676t
Bardet-Biedl syndrome,
182t
Bare lymphocytic syndrome,
734
“Barking” cough of croup,
1446
Baroceptors in respiration regulation,
1421
Barraquer-Simons syndrome,
2286
Barrier methods for contraception,
694
Bartonella bacilliformis,
982,
983f
Basal cell nevus syndrome,
e662-3
Base therapy for metabolic acidosis,
234
“Basic helix-loop-helix” (bHLH) proteins,
2112
Basic life support algorithm,
280f
Basilar-type migraine,
2042
Basketball, injuries in,
e684-2
“Bathing suit” melanocyte nevus,
2232f
Bath oil for skin disorders,
2216
Bathtub drowning,
24,
343
Bayley Scales of Infant Development (BSID-II),
126-127
B cells,
722
abnormalities of
inheritance in development of,
e117-6
in systemic lupus erythematosus,
843
BEACOPP regimen for Hodgkin lymphoma,
1742,
1743t
BEARS Sleep Screening Algorithm,
54t
Becker muscular dystrophy (BMD),
2119-2123
dilated cardiomyopathy with,
1630
laboratory findings in,
2120
Bedding, sudden infant death syndrome and,
1425
Bed sharing, sudden infant death syndrome and,
1425
Bee pollen for asthma,
271t
Behavior
effects of malnutrition on,
175t
emerging patterns of from 1 to 5 years of age,
32t
high-risk pregnancies and,
e89-1t
lead poisoning effects on,
2450
Behavioral development
during first year of life,
28t
Behavioral disorders/issues
See also Psychiatric disorders
assessment and interviewing for,
56-60
in children born to teen mothers,
701
in chronic illness,
e39-2
disruptive,
96-100,
97t
in childhood and adolescence,
99-100
in infancy and toddlerhood,
99
office intervention for,
16
in type 1 diabetes mellitus,
1986
Behavioral insomnia of childhood
sleep onset association type,
48
Behavioral observation audiometry (BOA),
2194
Behavioral states, newborn,
e7-2
Behavioral syndrome, neonatal,
625,
625f
Behavioral theories of development,
e6-4,
e6-5t
Behavioral therapy
for attention deficit/hyperactivity disorder,
110
Behavior rating scale,
110
Belladonna toxicity,
269t
Bell clapper deformity,
1861
Benign angiitis of central nervous system (BACNS),
876
Benign congenital hypotonia,
2119
Benign sleep myoclonus,
e587-5
Benzathine penicillin,
645t
for acute rheumatic fever prophylaxis,
924t
for group A streptococci infection,
918
for neonatal infection,
645t
for sexually transmitted infections in adolescents,
712t
Benzene, as inhalant,
681t
Benzocaine toxicity,
251t
Benzodiazepines
adverse effects of,
2031t
urine screening in adolescent use of,
676t
Berardinelli-Seip congenital lipodystrophy type 1 (BSCL1),
2286
Berardinelli-Seip congenital lipodystrophy type 2 (BSCL2),
2286
Bernard-Soulier syndrome,
1721
Best vitelliform degeneration,
2178
β-adrenergic agonists
for bronchopulmonary dysplasia,
e410-1
β-blockers
for long Q-T syndromes,
1618
for Marfan syndrome,
2445
for migraine prophylaxis,
2045
for systemic hypertension,
1645t
β-cells
hyperplasia in hyperinsulinemia,
521-522
microadenoma in hyperinsulinemia,
521-522
β-hemolytic streptococci,
636t
β-lactam antibiotics
mechanism of resistance to,
e173-1t
Bezoars,
1291
common medications implicated in,
257t
salicylates in formation of,
260
Bicarbonate (HCO
3−)
metabolic alkalosis and,
237
in respiratory acidosis,
238
Bicarbonate (HCO
3) buffer system,
e52-13
Bifunctional enzyme defect,
466t
Bile acid CoA ligase deficiency,
1385
Bile acids
disorders of transport, secretion, conjugation, and biosynthesis of,
1383-1384,
e346-4t
Bile acid synthetic defect (BASD),
1383t
Bile flow, cholestasis and functional abnormalities of,
1381
Bile salt export pump (BSEP) deficiency,
1383t,
1384
Bilevel continuous positive airway pressure (BiPAP)
for obstructive sleep apnea,
51
for respiratory distress and respiratory failure,
320
Biliary cirrhosis
as manifestation of liver disease,
1374
Bilious vomiting in intestinal malrotation,
1280-1281
Bilirubin
assessment in risk of jaundice,
605-606
in congenital dyserythropoietic anemia,
e446-1t
in graft
versus host disease,
761t
inherited deficient conjugation of,
1389-1390
normal neonatal values of,
605
Binge-purge type anorexia nervosa,
90
Bioavailability in drug therapy
Biobehavioral therapy for migraine,
2045
Biochemical testing in liver disease,
1379-1381
Bioequivalence of drug,
e57-2
Biofeedback for pain management,
371
Biologic agents
for juvenile idiopathic arthritis,
838t
Biomarkers in pharmacodynamics,
e57-9
Biophysical profile (BPP),
542,
543t
Biopsy
in chronic diarrhea,
1344
in fever of unknown origin,
902
kidney, in renal transplantation,
e530-5
myocardial, in heart transplantation monitoring,
e437-2
rectal suction, in Hirschsprung disease,
1285-1286
Biopsychosocial formulation in psychiatric diagnostic evaluation,
60
Biopsychosocial models
for eating disorder treatment,
94
Biotin,
194t,
196
dietary deficiency of,
433
for holocarboxylase synthetase deficiency,
432
Biotinidase deficiency,
432-433
secondary to pyruvate carboxylase deficiency,
506
Biphasic anaphylaxis,
817
Bird fancier or breeder lung,
1473
Birth asphyxia, cerebral palsy and,
2063-2064
Birth history
in neurologic evaluation,
e584-1
Birth injury
brachial plexus palsy due to,
2383
of spine and spinal cord,
573
Birthmarks, child abuse bruising
versus,
137
Bisacodyl suppositories,
74t
Bitemporal aplasia cutis congenita,
2222
Bites
due to abuse and neglect,
138
Black spot poison ivy,
2251
Bladder
calculi as complication of enterocystoplasty,
e536-2
congenital intestinal pseudo-obstruction and,
1283
control during preschool years,
33
Bladder neck obstruction,
1845
Bladder outlet obstruction,
1839t
Blalock-Taussig shunt,
1577
Blastomyces adhesion-1 (BAD-1),
1064
Bleeding time (BT)
in hemostatic disorders,
1697
reference values for,
1698t
Blindness
due to
Chlamydia trachomatis,
1035
night,
2154
due to vitamin A deficiency,
189
Blistering cutaneous porphyria,
e85-3
Block, heart
bundle branch, electrocardiographic assessment of,
1540
electrocardiography of first degree,
1540
first-degree,
1618
electrocardiography of,
1540
Blocking therapy for internal radiation contamination,
e699-5
Blood
multiple organ dysfunction syndrome and,
312t
shock-related dysfunction of,
307t
in stool, exclusion from day care due to,
e15-2t
Blood-borne infections in child care setting,
e167-2
Blood cholesterol screening,
479-480
Blood culture,
e164-1-e164-2
in fever of unknown origin,
902
in nontuberculous mycobacteria,
1015
in septic arthritis,
2399
Blood disorders
anemia(s) as,
1648-1650,
1648t
chronic hemolysis as,
1653
history and physical examination in,
1648-1649
laboratory studies in,
1649
parvovirus B19 infection-associated red cell aplasia as,
1652-1653
Pearson’s syndrome as,
1652
cardiac manifestations of,
1531t
hemorrhagic and thrombotic
acquired inhibitors of coagulation in,
1712-1713
clinical and laboratory evaluation of,
1696-1699
due to hereditary clotting factor deficiencies,
1699-1704
laboratory testing in,
1710
due to liver disease,
1712
platelet and blood vessel disorders as,
1714-1722
postnatal vitamin K deficiency as,
1712
in premature infants,
559t
in systemic lupus erythematosus,
843t
Blood flow
pulmonary, cyanotic congenital heart disease associated with,
1573-1596
in transitional circulation,
e415-1
Blood group incompatibility
ABO, hemolytic disease of newborn due to,
619
Blood lipids
cardiovascular disease and,
470
Blood loss
iron deficiency-anemia due to,
1656
in traumatic injury,
336t
Blood manifestations
due to cat-scratch disease,
985
in mitochondrial encephalomyopathy,
2065t
Blood pressure (BP)
adolescent assessment of,
666
in cardiac physical examination,
1533
in coarctation of the aorta,
1568
monitoring in respiratory distress syndrome,
586
in pediatric emergency assessment,
279
Blood smear
in congenital dyserythropoietic anemia,
e446-1t
in iron deficiency-anemia,
1657f
Blood studies in febrile seizure,
2018,
2036
Blood supply
to capital femoral epiphysis,
2356
Blood transfusion(s)
for erythroblastosis fetalis,
617-618
exchange
for erythroblastosis fetalis,
618
HIV transmission through,
1159
iron overload due to,
1675
Blood urea nitrogen (BUN)
in plasma osmolality,
e52-2
Bloody diarrhea,
Shigella in,
959
Bloody discharge from nipple,
e545-3
Blow-out orbital fracture,
2186
Blue diaper syndrome,
1319
Blue rubber bleb nevus,
2230
“Blue spells” in tetralogy of Fallot,
1574
Body image, eating disorders and,
93t
Body mass index (BMI),
180f-181f
in nutrition assessment,
172
Body surface area (BSA)
drug dosages based on,
e57-9
Bolus feeding of premature infant,
560
Bone(s)
cystic fibrosis and,
1494
effects of malnutrition on,
175t
Bone disease
See also Orthopedic problems
adynamic, in chronic kidney disease,
1825
due to bacillary angiomatosis,
986
metabolic
primary chondrodystrophy (metaphyseal dysplasia) as,
e695-1,
e695-1f
Bone infection,
2394-2398
nontuberculous mycobacterial,
1013
Staphylococcus aureus in,
905
Bone marrow culture in brucellosis,
981
Borderline lepromatous leprosy,
e208-2
Bosentan for pulmonary hypertension,
1602t
Botanical medicine, nutritional aspects of,
169
Botryoid rhabdomyosarcoma,
1760
Bottle, Mead Johnson,
1253
Bottle-feeding of premature infant,
560-562
Botulism immune globulin (BIG),
990
Bowel control during preschool years,
33
Bowel resection
short bowel syndrome due to,
1314
Bowman’s space, crescent formation in,
1778
Boys
first sign of puberty in,
649
Brachial plexus block for pain management,
371-372
Bracing
for Scheuermann disease,
2372
Bradyarrhythmias, emergency management of,
287,
288f
Bradypnea in pediatric emergency assessment,
280-281
Brain hemorrhage, due to hypernatremia,
214
Brain malformations
muscle development and,
2118
neonatal seizures due to,
2034
Brain natriuretic peptide (BNP) in pulmonary edema,
1469
Brainstem
multiple sclerosis effects on,
2077t
respiratory distress due to lesion of,
315t
Brainstem auditory-evoked responses (BAERs),
2192,
e584-11
Brainstem reflexes, brain death and,
e63-2
Brain tumor(s),
1746-1753
clinical manifestations of,
1747
complications and long-term management of,
1753
craniopharyngioma as,
1752
incidence and survival rates for,
1726t
secondary, due to radiation therapy,
e699-5t
Branched-chain ketonuria, hypoglycemia in,
528
Branchial cleft cysts and sinuses,
2221
Branching enzyme deficiency,
497
Breast
newborn assessment of,
536
surgical alterations to,
e545-4
trauma and inflammation of,
e545-2
Breast cancer,
e545-4
secondary, due to radiation therapy,
e699-5t
Breast-feeding,
160
collection of breast milk,
162
contraindications to,
161t
exclusive, for gastroenteritis prevention,
1338
growth of infant and,
162
HIV transmission through,
1159
inadequate milk intake,
161
medical contraindications to,
540,
540t
patterns of milk supply and,
160,
162t
sudden infant death syndrome and,
1425
ten steps to successful,
539t
type 1 diabetes mellitus and,
1972
Breath hydrogen test,
1306
Breathing
in newborn assessment,
535
in pediatric emergency assessment,
279-281
Breathing movements, fetal,
543t
Breathing patterns in newborn,
580
Breathlessness in asthma,
784t
Breath sounds in newborn,
535
Bright Futures Guidelines for Health Supervision of Infants, Children, and Adolescents,
14,
15f
Bromide
adverse effects of,
2031t
Bronchial carcinoid,
1504
Bronchial provocation testing,
768
Bronchiolectasis in cystic fibrosis,
1485
Bronchiolitis obliterans organizing pneumonia (BOOP),
e386-1
Bronchobiliary fistula,
1467
Bronchodilator therapy
for cystic fibrosis,
1493
Bronchoprovocation challenge,
784
Bronchopulmonary aspergillosis, allergic
immunoglobulin E levels in,
766
Bronchopulmonary dysplasia (BPD)
Bronchoscopic aspiration for atelectasis,
e402-1
Bronze baby syndrome,
611
Broviac catheter, infection with,
e172-1
Brown oculocutaneous albinism,
2238
Brown-Séquard syndrome,
2105
Bruton tyrosine kinase (Btk),
723,
724f
BSAP, infant botulism and,
989
B symptoms in Hodgkin lymphoma,
1741
Bulbar involvement in Guillain-Barré syndrome,
2143-2144
Bulbar palsies, due to botulism,
988,
989f
Bulk, muscle, assessment in neurologic examination,
e584-6
Bullae
of Stevens-Johnson syndrome,
2243f
Bullous congenital ichthyosiform erythroderma,
2270,
2270f
Bullous dermatosis of childhood, chronic,
2249,
2249f
Bullous pemphigoid (BP),
2248
Bumetanide
for acute renal failure,
1820
Bundle branch block,
1540
Bupropion
for attention deficit/hyperactivity disorder,
111t
for depression and anxiety symptoms,
63t
for weight loss in adults,
187t
Burkholderia cepacia,
977
Burkholderia pseudomallei,
e197-2
Burn(s),
349-357
as childhood injury,
23-24
complement system dysfunction in,
756
encephalopathy associated with,
2068
first aid measures for,
350
infections of
herpes simplex virus,
1103
nutritional support for,
354
oral ulceration due to,
1260t
psychologic adjustment to,
355
reconstruction and rehabilitation for,
355
Burst-forming unit-megakaryocytes (BFU-MK),
e440-1
Butane, as inhalant,
681t
1,4-Butanediol, adolescent abuse of,
675t
Butyl nitrate, as inhalant,
681t
γ-Butyrolactone, adolescent abuse of,
675t
Bypass strategies for neurodevelopmental dysfunction,
e29-7-e29-8
C
C3,
e127-1-e127-3
in acute poststreptococcal glomerulonephritis,
1784
in membranoproliferative glomerulonephritis,
1787
Cachexia, treatment of in palliative care,
157t
Caffeine for neonatal apnea,
581
Calcaneal apophysitis,
2418
Calcaneal stress fracture,
2418
Calcaneovalgus feet,
2336
Calcineurin inhibitors,
2217
in renal transplantation,
e530-4
Calcitonin in neuroendocrine tumor-associated diarrhea,
e333-2t
Calcitriol
for hypoparathyroidism,
1919
Calcium,
e41-17
conversion factors for,
e52-9t
in hyperparathyroidism,
1921
renal tubular regulation of,
e522-1
Calcium channel blockers (CCBs)
for pulmonary hypertension,
1602t
for systemic hypertension,
1645t
Calcium channelopathies,
2125t
Calcium chloride for resuscitation and arrhythmias,
294t
Calcium gluconate for hypoparathyroidism,
1919
Calcium salts
possible adverse reactions to in premature infant,
563t
Caloric intake
in bronchopulmonary dysplasia,
e410-1
in chronic kidney disease,
1824
for eating disorder treatment,
95
with “fast food” meal,
182
Caloric testing in neurologic examination,
e584-4
Calprotectin concentration in chronic diarrhea,
1344t
Camphor, toxicity of,
251t
Campylobacter,
968-970
clinical manifestations of,
969-970
inflammatory bowel disease
versus,
1298t
in traveler’s diarrhea,
1338t
Canadian immunization schedule,
895
Cancer antigen-125,
1872t
Candesartan for systemic hypertension,
1645t
Candida,
1053-1056
chronic mucocutaneous,
1056
after hematopoietic stem cell transplantation,
762
predisposition to infection due to immunodeficiency,
716t
in septic arthritis,
2398
in ungual and periungual infections,
1055
Cannabinoids
for neuropathic pain,
368t
urine screening in adolescent use of,
676t
Capillary hydrostatic pressure, pulmonary edema and,
1468
Capillary wedge pressure in shock,
311t
Capnocytophaga canimorsus,
e205-1
Capsular polysaccharide
group B streptococci,
926
Neisseria meningitidis,
932
Captopril
for systemic hypertension,
1645t
Carbamazepine
adverse effects of,
2031t
Carbamyl phosphate synthetase (CPS) deficiency,
448f,
449-451
Carbapenems,
e173-3
adverse reactions to,
826
Carbohydrates
adequate macronutrient distribution range for,
e41-1t
loading of for acute intermittent porphyrias,
e85-7
in oral rehydration solutions,
1335t
type 1 diabetes mellitus and intake of,
1981,
1982t
Carbohydrate-deficient glycoprotein syndrome,
1311
Carbohydrate metabolism, defects of,
493f,
494t-495t,
e81-1-e81-8
glycogen storage diseases as,
492-501
Fanconi-Bickel syndrome as,
499,
1318
glycogen synthetase deficiency as,
498
mimicking hypertrophic cardiomyopathy,
500
malabsorption due to,
1318
Carbon dioxide (CO
2)
lack of responsiveness to in bronchopulmonary dysplasia,
1521
partial pressure of,
e365-3f
in respiratory failure,
316
Carbon monoxide (CO)
diffusing capacity for,
e366-3
Carbon tetrachloride poisoning,
267
Carboplatin and cisplastin for cancer therapy,
e488-4t
Carcinogens, environmental,
e700-3
Carcinoid tumor,
e337-3
cardiac manifestations of,
1531t
Carcinoma
hepatocellular,
1772
in type II glycogen storage disease,
496
Card agglutination trypanosomiasis test (CATT),
1192
Cardiac arrest
potentially treatable conditions associated with,
289t
Cardiac arrhythmias
in
Corynebacterium diphtheriae-associated toxic cardiomyopathy,
e180-2
with Marfan syndrome,
2441
due to metabolic alkalosis,
237
Cardiac compressions in cardiopulmonary resuscitation,
291,
291f-292f
Cardiac glycoside-containing plants, toxicity with,
269t
Cardiac output (CO)
medications to maintain,
294t
Cardiac tamponade
cardiac arrest due to,
289t
as life-threatening injury,
336t
Cardiac teratogenic effects,
1527
Cardiomegaly in infants of diabetic mothers,
628
Cardiomyopathy
in Becker muscular dystrophy,
2119
Chagas disease-related,
1196
in chronic kidney disease,
1823t
in Duchenne muscular dystrophy,
2119
in plasma membrane carnitine transport defect,
460
toxic, due to diphtheria,
e180-3
Cardiothoracic ratio,
1537
Cardiovascular disease
failure to thrive in,
148t
in mucopolysaccharidoses,
515t
of peripheral vascular system
arteriovenous fistula as,
e438-1
phosphorylase kinase deficiency as,
498
in premature infants,
559t
psychopharmacology and,
65
renal transplantation and,
e530-2
respiratory signs and symptoms of,
e413-1t
Cardiovascular manifestations,
1532t
in lysosomal storage disorders,
485t
in mitochondrial encephalomyopathy,
2065t
in systemic inflammatory response syndrome,
309t
in systemic lupus erythematosus,
843t
Cardiovascular medication poisoning,
261-263
Cardiovascular system
inhalation anesthetic effects on,
e70-6
management of in drowning,
345
preanesthetic assessment of,
e70-13
shock-related dysfunction of,
307t
transition from fetal to neonatal circulation in,
1529,
e415-1f
Cardioversion, synchronized,
288-289
Carditis
in acute rheumatic fever,
922
Care settings for palliative care,
151
Carnitine acylcarnitine translocase (CACT) deficiency,
457t
Carnitine-acylcarnitine translocase (CACT) deficiency,
461
Carnitine deficiency
cardiac manifestations of,
1531t
Carnitine palmitoyltransferase (CPT) deficiency,
2132
Carnitine palmitoyltransferase-IA (CPT-IA) deficiency,
461
Carnitine palmitoyltransferase-I (CPT-I) deficiency,
457t
Carnitine palmitoyltransferase-II (CPT-II) deficiency,
457t,
461
Carnitine transporter deficiency,
457t
Carpal bones, centers of ossification appearance in,
29t
Carpenter syndrome
congenital heart disease with,
1531t
Carrier detection in immunodeficiencies,
e117-6
Cartilage matrix proteins, skeletal dysplasias of,
2424-2427
Carvedilol
for systemic hypertension,
1645t
Caseating granuloma in nontuberculous mycobacteria,
1012
Casting, serial, for clubfoot,
2337
Catabolic losses in diabetes mellitus,
1980
Catalase,
Staphylococcus aureus production of,
904
Catalase-positive organism,
745
Catamenial pneumothorax,
1509
Catarrhal stage of pertussis,
945
Catch-up immunization schedule,
889,
890f
Catheter ablation for supraventricular tachycardia,
1614-1615
Catheter infection
coagulase-negative staphylococcal,
910
Catheterization
umbilical artery
in respiratory distress syndrome,
586
risks associated with,
587
Catheter-related bloodstream infection (CRBSI),
903,
e172-1
Caudal regression syndrome,
1356
CD2, development and differentiation of,
e117-1
CD3
development and differentiation of,
e117-1
CD4
development and differentiation of,
e117-1
interaction with other immune cells,
e117-5
CD7, development and differentiation of,
e117-1
CD8
development and differentiation of,
e117-1
in Epstein-Barr virus,
1111
interaction with other immune cells,
e117-5
CD10, development and differentiation of,
e117-2
CD19, development and differentiation of,
e117-2
CD22, development and differentiation of,
e117-2
CD23, development and differentiation of,
e117-2
CD40
development and differentiation of,
e117-2
interaction with other immune cells,
e117-5
CD40 ligand, mutations in,
726
CD45
interaction with other immune cells,
e117-5
CD54, interaction with other immune cells,
e117-5
CD58, interaction with other immune cells,
e117-5
CD73, development and differentiation of,
e117-2
CD154, interaction with other immune cells,
e117-5
CDC
See Centers for Disease Control and Prevention (CDC)
Cefazolin,
e173-4t-e173-11t
for infective endocarditis,
1625t
for infective endocarditis prophylaxis,
1626t
for neonatal infection,
645t
for septic arthritis,
2400
for
Staphylococcus aureus,
907t
Cefixime,
e173-4t-e173-11t
for
Salmonella gastroenteritis,
953t
for sexually transmitted infections in adolescents,
712t
for
Shigella infection,
961
Cefotaxime,
e173-4t-e173-11t
for meningococcal disease,
933t
for neonatal infection,
645t
for pneumococcal meningitis,
913
for
Salmonella gastroenteritis,
953t
for septic arthritis,
2400
Ceftriaxone,
e173-4t-e173-11t
for infectious diarrhea,
1337t
for infective endocarditis,
1625t
for infective endocarditis prophylaxis,
1626t
for meningococcal disease,
933t
for
Neisseria meningitidis prophylaxis,
934t
for neonatal infection,
645t
for
Salmonella gastroenteritis,
953t
for sexually transmitted infections in adolescents,
712t
for
Shigella infection,
961
Celecoxib
for pain management,
364t
Celiac plexus nerve block,
372
Cellular immunodeficiencies,
728-730,
728t
autoimmune polyendocrinopathy-candidiasis ectodermal dysplasia as,
730
CD8 lymphocytopenia as,
730
defective cytokine production as,
729
defective expression of T-cell receptor-CD3 complex as,
729,
729f
Cellulitis,
2300-2301
of auricle and external auditory canal,
2198
Haemophilus influenzae in,
942
Central auditory processing disorders,
2188
Central chemoreceptors in respiration regulation,
e365-15
Central cord syndrome,
2103
Central giant cell granuloma of jaw,
e308-1
Central hearing loss,
2188
Central nervous system (CNS)
See also Neurologic entries
mushroom poisoning effects on,
e703-2
in Neonatal Intensive Care Unit Neurobehavioral Scale,
624t
of premature infants,
559t
prenatal development of,
e6-7f
Central nervous system (CNS) disorders,
565
brain tumor(s) as,
1746-1753
clinical manifestations of,
1747
complications and long-term management of,
1753
craniopharyngioma as,
1752
incidence and survival rates for,
1726t
secondary, due to radiation therapy,
e699-5t
infection as,
2086-2098
Blastomyces dermatitidis,
1064
Listeria monocytogenes,
e181-2
neonatal seizures due to,
2034
Pseudomonas aeruginosa,
976t
Rocky Mountain spotted fever,
1042
Staphylococcus aureus,
905
stroke-like events
versus,
2085
pulmonary manifestations of,
e413-1t
respiratory acidosis due to,
239,
241t
respiratory distress due to,
315t,
316
of spine and spinal cord, due to birth,
573
Central nervous system (CNS) manifestations
in hemolytic-uremic syndrome,
1793
in mitochondrial encephalomyopathy,
2065t
Central nervous system (CNS) therapy for acute lymphocytic leukemia,
1735
Central pontine myelinolysis (CPM),
218
Central venous catheter (CVC)
fever without a focus in,
896t
infection with,
e172-1
due to coagulase-negative staphylococci,
910
Central venous pressure in shock,
311t
Centromere antibody in rheumatic disease,
e147-3t
Cephalexin for impetigo,
2300
Cephalic vein, venous access in,
292,
295f
Cephalometric radiograph,
1261
Cephalosporins,
e173-3
for group A streptococci infection,
918
for neonatal infection,
644
for sexually transmitted infections in adolescents,
712t
Cereal-based oral rehydration,
1334
Cerebellar astrocytoma,
1748t
Cerebellar ataxia,
2054
varicella-zoster virus in,
1109
Cerebellar hypoplasia,
2118
Cerebellar pathways, multiple sclerosis effects on,
2077t
Cerebellar vermis, agenesis of,
2054
Cerebellum
multiple sclerosis effects on,
2077t
Cerebral blood flow (CBF),
297f
Cerebral edema
with fulminant hepatic failure,
1414
due to type 1 diabetes mellitus,
1981
Cerebral palsy (CP),
2061-2065
intellectual disability
versus,
126
Cerebral perfusion pressure (CPP),
296
cerebral blood flow and,
297f
Cerebral salt wasting,
1884t
Cerebral thrombosis, with tetralogy of Fallot,
1576
Cerebrospinal fluid (CSF)
latex agglutination testing on,
e164-1
Cerebrospinal fluid (CSF) examination,
e164-2
in central nervous system infections,
2088t
in coccidioidomycosis,
1066
in enteroviral meningitis,
1091
in meningococcal meningitis,
932
in poliovirus infection,
1084
Cerebrospinal fluid (CSF) shunts, infections associated with,
910,
e172-1-e172-2
Cerebrum, multiple sclerosis effects on,
2077t
Ceroid lipofuscinosis, infantile,
484t
Certification of pediatricians,
12
Cervical culture in gonococcal disease,
938
Cervical lymphadenopathy
Corynebacterium diphtheriae,
e180-2f
as sign of childhood cancers,
1730f
Cervical spine
juvenile idiopathic arthritis involvement in,
832,
834f
Cervix
maternal testing of,
543t
Cesarean section,
e89-4
maternal HIV infection and,
1159
Cetirizine
for urticaria and angioedema,
815t
Chamomile, German, for sedation,
271t
Chanarin-Dorfman syndrome,
2272
Channelopathies,
2125t
in long and short Q-T syndrome,
1617t
strokelike events
versus,
2086
sudden infant death syndrome and,
1423t,
1426
Chaotic atrial tachycardia,
1615
Chelation therapy
for internal radiation contamination,
e699-5
Chemical burn
oral ulceration due to,
1260t
Chemical conjunctivitis,
2168
Chemical pleurodesis for pneumothorax,
1511-1512
Chemoprophylaxis
acute rheumatic fever,
924t
Chemotherapy,
e488-1-e488-5,
e488-2f-e488-3f
as cancer risk factor,
1727t
hypersensitivity to agents used in,
826
hypogonadism due to,
1945
infections associated with,
e488-5t
malabsorption due to,
1314
neutropenia associated with,
1055
vomiting with, therapy for,
1244t
Chest
computed tomography and magnetic resonance imaging of,
e366-2
life-threatening injuries to,
336,
336t
Chest compressions in cardiopulmonary resuscitation,
291,
291f-292f
Chest pain
differential diagnosis of,
1530t
as manifestation of extrapulmonary disease,
1526,
e413-1t
Chest radiography
in cardiac assessment,
1537
in respiratory disease diagnosis,
e366-2
in total anomalous pulmonary venous return,
1589,
1590f
Chest tube for emergencies,
295
Chief complaint in neurologic evaluation,
e584-1
Chigger bite,
2320
scrub typhus due to,
1045
Child care,
e15-1-e15-5
antibiotic use and bacterial resistance and,
e167-2
consultation and partnering with providers of,
e15-5
developmental outcomes and,
e15-3
eating in setting of,
165
licensing, regulation, and accreditation of,
e15-1
Child mortality,
1-2
worldwide indicators of,
3t
Child Protective Services (CPS),
141
Child-rearing practices,
2-3
Children’s Oncology Group (COG),
1732
on Wilms tumor treatment,
1759
Children’s Yale-Brown Obsessive-Compulsive Scale (C-YBOCS),
80
Child restraint in motor vehicles,
21,
21f,
21t
China, migrant population in,
7
Chinese herbal medications,
805
Chiropractic treatment,
273
Chlamydia trachomatis,
1035-1038
lymphogranuloma venereum due to,
1038
prophylaxis following rape,
704,
704t
Chloramphenicol,
e173-4t-e173-11t,
e173-13
for
Bartonella infection,
983
for cystic fibrosis lung infection,
1492t
for louse-borne typhus,
1048
for meningococcal disease,
933t
for neonatal infection,
645t
possible adverse reactions to in premature infant,
563t
Chloride
in oral rehydration solutions,
1335t
Chloride channelopathies,
2125t
Chloride-losing diarrhea, congenital,
223
Chloroquine
for porphyria cutanea tarda,
e85-12
Chlorothiazide
for systemic hypertension,
1645t
Chlorpheniramine for allergic rhinitis,
777t-778t
Chlorpromazine
for chemotherapy-associated vomiting,
1244t
for pain management,
364t
Chlorthalidone for systemic hypertension,
1645t
Cholangiography
in liver dysfunction,
1379
magnetic resonance, in sclerosing cholangitis,
e352-1
Cholangiopancreatography, endoscopic retrograde,
1379
Cholangitis
sclerosing, with inflammatory bowel disease,
e352-1
Cholera,
965-968
clinical manifestations of,
966,
967f
diagnosis and differential diagnosis of,
967
laboratory findings in,
966
Cholestasis
differential diagnosis of,
1377t
as manifestation of liver disease,
1374
with total parenteral nutrition,
e352-2
Cholesterol
disorders of intracellular metabolism of,
478-479
adrenocortical insufficiency due to,
1926
high-density lipoproteins and reverse transport of,
473
in steroid biosynthesis,
e568-1
Cholesterol ester storage disease (CESD),
479,
491
Cholesterol gallstones,
e358-1
Cholesterol granuloma of tympanic membrane,
2212
Cholesteryl ester transfer protein (CETP) deficiency,
477
Choline magnesium salicylate for pain management,
364t
Cholinesterase-inhibiting insecticide poisoning,
266-267
Chondrodysplasia, Jansen-type metaphyseal,
1923
Chondrodysplasia punctata (CPD),
2272
Chondromalacia patella,
2354
Chorea-acanthocytosis,
2057t
Chorionic gonadotropin, human
in ovarian carcinomas,
1872t
Chorionic villus sampling,
543t
Choroid plexus
fetal cysts, ultrasound of,
550t
Christmas tree pattern,
2262
Chromones for allergic disease,
771-772
Chromosomal abnormalities
in acute myeloid leukemia,
1738t
Chromosomal disorders,
381
chromosome instability syndromes as,
412
severe intellectual disability in,
123t
sex chromosome aneuploidy as,
408-410,
409t
Klinefelter syndrome as,
410
of structure,
404-408
marker and ring chromosomes as,
408
Chromosome 22q11.2 deletion,
2382
Chronic compartment syndrome (CCS),
2416-2417
Chronic disease
adolescent, ethical considerations regarding,
e3-5
Crohn disease appearance as,
1302
in foster care children,
e35-2t
Chronic infantile neurologic cutaneous and articular disease (CINCA),
855t,
858
Chronic myelogenous leukemia (CML),
748t,
1738-1739
hematopoietic stem cell transplantation for,
758
Chronic progressive external ophthalmoplegia (CPEO),
391t,
2131-2132
Chronic renal failure, rickets due to,
205-206
Chronic respiratory failure,
1519
Chronic suppurative otitis media (CSOM),
2210
Chylomicron retention disease,
1313
Chymotrypsin,
e339-3
concentration of in chronic diarrhea,
1344t
Cicuta species toxicity,
269t
Cigarette smoking
allergic reaction to,
769
porphyria cutanea tarda and,
e85-11
as sudden infant death syndrome risk factor,
1424
wheezing and bronchitis and,
1460
Cimetidine
for
Helicobacter pylori gastritis,
1293t
for urticaria and angioedema,
815t
Circadian rhythm in sleep,
46
Circulation
in pediatric emergency assessment,
281
Circulatory collapse, malarial,
1206
CIRH1A gene defect,
1383t
Cirrhosis
biliary
as manifestation of liver disease,
1374
as manifestation of liver disease,
1374
portal hypertension with,
e359-1
Cisapride, possible adverse reactions to in premature infant,
563t
Cisatracurium for intubation,
321t
Cis-regulatory genomic sequences,
e320-1
Citalopram
for depression and anxiety symptoms,
63t
for premenstrual dysphoric disorder,
692t
Clarithromycin,
e173-3,
e173-4t-e173-11t
for
Chlamydophila pneumoniae,
1035
for
Helicobacter pylori gastritis,
1293t
for infective endocarditis prophylaxis,
1626t
for
Legionella infection,
e200-2
for Mediterranean spotted fever,
1044
for
Mycobacterium avium complex prophylaxis,
1175t-1176t
for
Mycoplasma pneumoniae,
1031
for nontuberculous mycobacterial prophylaxis,
1015-1016
for vulvovaginitis,
1868t
Clasp-knife phenomenon,
e584-6
Clavicular fracture,
2392
as delivery room emergency,
578-579
Clean-contaminated wound, perioperative prophylaxis and,
e166-2,
e166-4t
Cleansing, acne and,
2323
Clear cell sarcoma of kidney (CCSK),
1760
Cleidocranial dysplasia,
2431,
2432f
oral manifestations of,
1254
Clinical geneticist,
382t
Clinical Laboratory Improvement Amendments (CLIA) of 1988
on office bacteriology,
e164-3
Clinical Risk Index for Babies (CRIB),
563
Clinical trials
for childhood cancer,
1732
Clofazimine
for
Mycobacterium leprae,
e206-4
Clomipramine
for depression and anxiety symptoms,
63t
for premenstrual dysphoric disorder,
692t
Clonazepam
for depression and anxiety symptoms,
63t
for neuroirritability in palliative care,
155t-156t
Clonidine
for attention deficit/hyperactivity disorder,
111t
for neuroirritability in palliative care,
155t-156t
for systemic hypertension,
1645t
Closed-loop intestinal obstruction,
1287-1289
Clostridium botulinum,
987-991
poliovirus infection
versus,
1085t
Clostridium difficile infection (CDI),
994-995
inflammatory bowel disease
versus,
1297,
1298t
Clostridium difficile toxin,
1313
Clothes, work, chemical pollutants in,
e700-3
Clubbing
digital
nonpulmonary disease associated with,
e366-2t
Clusters of differentiation,
e117-1
Coagulase,
Staphylococcus aureus production of,
904
Coagulase-negative staphylococci (CONS),
909-910
Coagulation proteins,
1694
Coagulopathy(ies)
with fulminant hepatic failure,
1414
hematuria associated with,
1796
hypothyroidism-associated,
1903t
Coal tar preparations,
805
Cobblestoning in vernal conjunctivitis,
810,
810f
Coca Cola, diarrhea and,
1335t
Codeine
equianalgesic doses and half-life of,
367t
for pain management,
365t
urine screening in adolescent abuse of,
676t
Coefficient of variation (CV),
2466
Cognitive assessment in communication disorder,
120
Cognitive-behavioral therapy (CBT),
66
for chronic fatigue syndrome,
e115-3
for obsessive-compulsive disorder,
80-81
Cognitive complications
of congenital diaphragmatic hernia,
596
in sickle cell disease,
1669
Cognitive development,
e6-3-e6-4
age 12-18 months,
31,
32t
during first 2 years,
27t
during preschool years,
34
Cognitive distortions, suicide and,
88
Cognitive function
elementary school success and,
37-38,
37t
in type 1 diabetes mellitus,
1986
Cognitive theories of development,
e6-4
Colchicine for familial Mediterranean fever,
857
Colchicum autumnlae toxicity,
269t
Cold-induced fat necrosis,
358
Coleus forskohlii for asthma,
271t
Colic, home remedies among African Americans for,
e4-2t
Co-lipase deficiency,
1306t
Collagen, type I, defects in,
2437
Collagenosis, reactive perforating,
2279,
2279f
Collapse-consolidation in tuberculosis,
998,
1000f
Collateral ligament injury,
2414
Colon
mega-, in Chagas disease,
1196
Colonization
bacterial in neonate,
630
Colony-forming unit-megakaryocytes (CFU-MK),
e440-1
Color Doppler echocardiography,
1568
Color vision testing,
2149
Coma
nonketotic hyperosmolar,
1981
pentobarbital, for status epilepticus,
2039t
in traumatic brain injury,
298
Combination vaccines,
889
Combined immunodeficiency (CID),
730-738,
731t
enteroviral meningoencephalitis with,
1092
“Coming out” by transgender adolescents,
656-657
Comminuted fracture,
2388f
Committee on Infectious Diseases (COID),
885
Committees, pediatric ethics,
e3-4
Common innocent murmur,
1536
Communication
about life-threatening or life-altering illness,
151-152,
e3-1
in autistic disorder,
100
during first 2 years,
27t
in post-resuscitation care,
296
in transport medicine,
e61-7
Communication disorders,
114-122
in Asperger’s syndrome,
118
in autism and pervasive developmental disorders,
118
clinical manifestations of,
117
comorbid psychiatric disorders,
121
dysfluency (stuttering, stammering) as,
122,
122t
isolated expressive language disorder as,
118
in mental retardation,
118
pragmatic language disorder as,
118
specific language impairment as,
117-118
Community
chronic illness and,
e39-3
obesity prevention in,
187t
well child care and,
16-17
Comparative genomic hybridization (CGH),
376,
377t,
396
Compartment(s)
in pharmacokinetics,
e57-2
pulmonary edema and,
1468
Compassionate care for foster care children,
e35-2t
Compensatory respiratory alkalosis,
230
Compensatory scoliosis,
2371
Complaints, psychosomatic illness and,
68
Complementary and alternative medicine,
270-274
massage and other bodywork therapies,
273
nutritional aspects of,
169
Spanish-English botanical name translation chart,
274t
Complement fixation (CF) test,
e219-1
Complement in serum sickness,
819
Complement system,
e127-1-e127-3,
e127-2f
alternative pathway of,
e127-2
disorders of
fever without a focus in,
896t
of plasma, membrane, or serosal control proteins,
755
membrane attack complex in,
e127-2
in neonatal immunity,
631
Complete blood count (CBC)
in immunodeficiency screening,
718t
Complex febrile seizure,
2017
Complex partial seizure,
2021
Compliance
respiratory,
322
assessment in mechanical ventilation,
328
diseases associated with decreased,
323
Composite graft in intestinal transplantation,
e331-1
Compressions, chest, in cardiopulmonary resuscitation,
291,
291f-292f
Computed tomography angiography (CTA)
Computed tomography (CT)
in fever of unknown origin,
902
in liver dysfunction,
1379
in neurologic examination,
e584-9
in orthopedic problems,
2335
in septic arthritis,
2400
in urinary tract obstruction,
1841
in X-linked adrenoleukodystrophy,
468,
469f
Computed tomography venography (CTV),
2083,
2083f
Concrescence, tooth,
1250
Conditioning therapy for nocturnal incontinence,
1852
Conduction disorder following tetralogy of Fallot repair,
1577-1578
Confidentiality of adolescent medical information,
e106-2
Conformal irradiation,
1732
Confusional arousal,
51-52
Congenital adrenal hyperplasia (CAH),
1930-1939,
1931f
adrenocortical insufficiency due to,
1924,
1925t
due to 3β-hydroxysteroid dehydrogenase deficiency,
1936
disorders of sex development due to,
1962
metabolic alkalosis in,
236
Congenital anemia, hypoplastic,
1650-1651
Pearson’s syndrome as,
1652
Congenital anomalies,
e92-2,
e92-3t
of central nervous system,
1998-2013
muscle development and,
2118
congenital heart disease with,
1531t
in infants of diabetic mothers,
628
of lung,
1463-1467
agenesis and aplasia as,
1463
bronchobiliary fistula as,
1467
cystic adenomatoid malformation as,
1464,
1465f
lymphangiectasia as,
1467
of respiratory tract, wheezing due to,
1457
Congenital anorchia,
1944
Congenital cranial nerve dysinnervation disorders (CCDD),
2006
Congenital cystic adenomatoid malformation (CCAM),
1464,
1465f
Congenital enterocyte heparin deficiency (CEHD),
1311
Congenital fibrosis of extraocular muscles (CFEOM),
2006
Congenital glutamine deficiency,
445
Congenital heart disease (CHD)
acyanotic
absence of pulmonary valve as,
1571
aorticopulmonary window defect as,
1561
atrial septal defect as,
1551
coronary-cameral fistula as,
1561
mitral valve prolapse as,
1572
partial anomalous pulmonary venous return as,
1553-1554
pulmonary valvular insufficiency as,
1571
regurgitation lesions as,
1571
sinus venosus atrial septal defect,
1553
supracristal ventricular septal defect with aortic insufficiency as,
1559
tricuspid regurgitation as,
1572
cyanotic
abnormal position of heart and heterotaxy syndromes as,
1595-1596
associated with decreased pulmonary blood flow,
1573-1585
associated with increased pulmonary blood flow,
1585-1596
single ventricle as,
1592
fever without a focus in,
896t
infective endocarditis and,
1622
respiratory signs and symptoms of,
e413-1t
sudden death due to,
1619
Congenital hypotonia, benign,
2119
Congenital ichthyosiform erythroderma
Congenital insensitivity to pain and anhidrosis,
2143
Congenital lobar emphysema (CLE),
1461
Congenital Lyme disease,
1027
Congenital muscle fiber-type disproportion (CMFTD),
2115
Congenital muscular torticollis (CMT),
2377-2379
Congenital myasthenic syndrome with episodic apnea (CMS-EA),
2133,
2133t
Congenital mydriasis,
2155
Congenital nasolacrimal duct obstruction (CNLDO),
2165
Congenital neutropenia, severe,
750
Congenital ocular motor apraxia,
2161
Congenital secondary polycythemia,
e461-1
Congenital sideroblastic anemia,
e450-1f
Congenital vitamin D deficiency,
205
Conium maculatum toxicity,
269t
Conjugated bilirubin,
1375
Conjunctivitis,
2166-2169,
2167t,
2168f-2169f
Haemophilus influenzae,
943
hemorrhagic, due to enterovirus,
1091
herpes simplex virus,
1101
purulent, exclusion from day care due to,
e15-2t
tularemia inoculation,
978
Conjunctivitis otitis media syndrome,
2205
Connective tissue disease
cardiac manifestations of,
1531t
Connective tissue nevus,
2235
Conotruncal heart defects,
1527
Consolidation treatment for acute lymphocytic leukemia,
1735
Constitutional growth delay,
1880
Constrictive pericarditis,
1637
Consultation, ethics,
e3-4
Contact allergy, involving eyes,
810
Contact factors deficiency,
1703
Contact lenses for hyperopia,
2151
Contaminated wound, perioperative prophylaxis and,
e166-2,
e166-4t
Contiguous gene deletion syndrome,
406
Contiguous gene disorders,
381
Contingent responses, development and,
e6-2
Continuing education for emergency medical services for children,
e61-1
Continuity of care
for children in foster care,
e35-2t
for chronic illness,
e39-3
Continuous gene deletion syndrome,
2269
Continuous glucose monitoring (CGM),
1983-1984
Continuous glucose monitoring system (CGMS),
1983
Continuous heart murmur,
1535
Continuous positive airway pressure (CPAP)
for obstructive sleep apnea,
51
for respiratory distress and respiratory failure,
320,
585
Continuous renal replacement therapy (CRRT),
1822
Continuous subcutaneous insulin infusion (CSII),
1977
Continuum of care model in emergency medical services for children,
e61-12
Contraception,
692-699,
695t
combination methods for,
696
counseling regarding,
694
intrauterine devices for,
699
minors right to consent for,
e106-2
special needs girls and,
1875
for women with congenital heart disease,
1609
Contraceptive patch, for special needs girls,
1875
Contraceptive ring,
697
special needs girls and,
1875
Contraction stress test (CST),
542,
543t
Contractures
in Becker muscular dystrophy,
2119
congenital, orthopedic management of,
e674-3
in Duchenne muscular dystrophy,
2119
in neuromuscular disorders,
2109
Contrast radiography in gastroesophageal reflux disease,
1267,
1267f
Control, preschoolers need for,
35-36
Controllers in respiration regulation,
e365-15
Control proteins, complement, deficiencies of,
754t,
755
Control variable in mechanical ventilation,
324-325
Contusion
lumbar disk, as sports injury,
2412
Convalescent stage of pertussis,
945
Convective heat loss in newborn,
536-537
Conventions, international, for protection of children from effects of war,
e36-6
Convergent retractorius,
2161
Conversion disorder,
68t,
69
Convex lenses for hyperopia,
2151
Coping styles
psychosomatic illness and,
68
in type 1 diabetes mellitus,
1986
Copper-histadine therapy,
2075
COPP regimen for Hodgkin lymphoma,
1742,
1743t
Coproporphyrinogen oxidase (CPO),
e85-2f
Copy number variations (CNVs),
399,
e56-1
Cornea
open globe injury and,
2185
superficial abrasions of,
2184
Corneal manifestations of system disease,
e619-3
Corneal reflex
in strabismus diagnosis,
2157
Cornelia de Lange syndrome,
2007t
Cornstarch for type I glycogen storage disease,
495
Coronal plane deformities,
2348
Coronary artery(ies)
aneurysm of in Kawasaki disease,
864,
865f
sudden death and anomalies of,
1619
Coronary-cameral fistula,
1561
Coronary heart disease (CHD),
459
Corporal punishment, abuse
versus,
135
Cortical dysplasian focal,
2004
Cortical necrosis, renal,
1818
Corticosteroid-binding globulin deficiency (CBG),
1926
Corticosteroids
adrenal insufficiency due to abrupt cessation of,
1929
adverse effects, risk assessment for,
795t
for chronic granulomatous disease,
746
for Diamond-Blackfan anemia,
1651
for juvenile dermatomyositis,
849
for pulmonary hemosiderosis,
1500
for respiratory distress syndrome,
586
antenatal, for prevention of,
584
for systemic lupus erythematosus,
844
Corticotropin deficiency,
1929
Corticotropin-releasing hormone (CRH),
e568-3
Cortisol
in adrenal insufficiency,
1928
in Cushing syndrome,
1940
decreased binding affinity of,
1926
Corynebacterium minutissimum,
2306
Corynebacterium ulcerans,
929
Costeff optic atrophy syndrome,
433
Costs
of antiseizure therapy,
2028
of chronic illness in childhood,
e39-2
Cough
as manifestation of extrapulmonary disease,
1526
as prominent finding in disorders,
1460t
in respiratory syncytial virus infection,
1128
Cough reflex, brain death and,
e63-2t
Counseling
genetic,
377-379,
378t
in acute intermittent porphyrias,
e85-8
in chronic granulomatous disease,
746
in congenital heart disease,
e418-3
in erythropoietic protoporphyria,
e85-17
in neurofibromatosis,
2048
in peroxisomal disorders,
467
in transmissible spongiform encephalopathies,
e270-4t
in X-linked adrenoleukodystrophy,
470
in intellectual disability management,
129
for neurodevelopmental dysfunction,
e29-8
Counter-regulatory hormones,
518
Cow’s milk
type 1 diabetes mellitus and,
1972
Cow’s milk protein-based formula,
163
Coxsackie,
1088t
in myocarditis and pericarditis,
1091
Cranial ultrasonography,
e584-9
Craniofrontonasal dysplasia,
2012t
Craniovertebral junction, pathologic conditions at,
2381
Creatine kinase (CK)
in neuromuscular disorders,
2110
Creatinine in posterior urethral valves,
427
Crescent formation in Bowman’s space,
1778
Crescentic progressive glomerulonephritis,
1789-1790
Cri-du-chat syndrome,
2007t
Critical aortic stenosis,
1565
Critical high airway obstruction syndrome (CHAOS),
577,
578f
Critical illness
See also Acute illness
polyneuropathy in, poliovirus infection
versus,
1085t
“Critical sample” in hyperinsulinemia,
521,
522t
Cromolyn sodium
for allergic conjunctivitis,
811t
for allergic rhinitis,
780t
Crossed adductor response,
e584-7
Crossing over, genetic,
395
Cross-Kusick-Breen syndrome,
2239
Crotalidae-specific Fab antibodies,
258t
Crouzonomesodermoskeletal syndrome,
2012t
Crush injury of phalanx,
2391
Crusts, examination of,
e637-1
Crying during age 0-2 months,
27
Cryotherapy
for sexually transmitted infection,
713t
Cryptogenic epilepsy,
2013
Crystalloids for anaphylaxis,
818t
Cubital vein, venous access in,
292,
295f
Cuff, blood pressure,
1533
Cultural encounters,
e4-4
Cultural factors/issues
in high-risk pregnancies,
e89-1t
in psychosomatic illness,
67
Cultural groups, newly recognized,
e4-3
Cultural practices, bruises caused by,
137-138
Culture
bone marrow in brucellosis,
981
cervical in gonococcal disease,
938
genital,
e164-2
in
Chlamydia trachomatis infection,
1036
in
Haemophilus influenzae,
941
in parainfluenza viruses,
1125t
pharyngeal in gonococcal disease,
938
rectal swab
in
Campylobacter infection,
970
in
Shigella infection,
960
sputum in tuberculosis,
1003
stool
in
Campylobacter infection,
970
in
Clostridium difficile infection,
995
in infectious enteritis,
1334
in
Shigella infection,
960
Culture of medical profession,
e4-3
Cushion defect, endocardial,
1554
Cutaneous hydration for atopic dermatitis,
804
Cutaneous lymphocyte-associated antigen (CLA),
802
Cutaneous polyarteritis nodosa,
872-874
Cutis verticis gyrata,
2222
Cyanosis
abnormal hemoglobins causing,
1672
as manifestation of extrapulmonary disease,
1526,
e413-1t
physical examination of,
1531
Cyanotic congenital heart disease
abnormal position of heart and heterotaxy syndromes as,
1595-1596
associated with decreased pulmonary blood flow,
1573-1585
associated with increased pulmonary blood flow,
1585-1596
double-outlet right ventricle as,
1582
with malposition of great arteries,
1588-1589
with pulmonary stenosis,
1588
extracardiac complications of,
1603t
respiratory distress syndrome
versus,
583-584
single ventricle as,
1592
transposition of the great arteries as
with ventricular septal defect,
1587
with ventricular septal defect and pulmonary stenosis as,
1574,
1583f
Cyclo-oxygenase (COX) inhibitor poisoning,
260
Cyclo-oxygenase 2 (COX-2) inhibitors for rheumatic disease,
e148-3
Cyclophosphamide
for lupus nephritis,
1788
for nephrotic syndrome,
1805
Cyclosporine
for atopic dermatitis,
805
diabetes associated with,
1997
gingival overgrowth due to,
1257
for nephrotic syndrome,
1805
for urticaria and angioedema,
815t
Cyproheptadine
for Cushing syndrome,
1941
for migraine prophylaxis,
2044t
for vomiting prophylaxis,
1244t
Cyst(s)
branchial cleft and thyroglossal,
2221
epidermal inclusion,
2328
gingival of newborn,
2298
Cystathionine β-synthase (CBS) deficiency,
425-427
Cysteine/cystine, defects in metabolism of,
429
Cystic abdominal masses in newborn,
535
Cystic dysplasia, renal,
1827
Cystic fibrosis (CF),
1481-1497
dental problems associated with,
1251t
diabetes related to,
1996
metabolic alkalosis due to,
236
neonatal screening for,
2466
newborn screening for,
1490
pancreatic insufficiency in,
1369
Pseudomonas aeruginosa in,
976
skin manifestations in,
2330
urinary lithiasis with,
e541-2
Cystic fibrosis-related diabetes (CFRD),
1996
Cystic fibrosis transmembrane conductance regular protein (CFTR)
Cystitis,
1830
infectious causes of,
1799
Cystography in vesicoureteral reflux,
1836
Cystourethrogram, voiding
in urinary tract obstruction,
1840
Cytarabine for cancer therapy,
e488-4t
Cytochrome C oxidase,
1406
Cytochrome C oxidase deficiency myopathy, reversible infantile,
2066-2067
Cytochrome P450 system
in adrenal biosynthesis,
1923
porphyria cutanea tarda and,
e85-11
Cytogenetics,
394-414
abnormalities of chromosomal number in,
399-403
abnormalities of chromosomal structure in,
404-408
marker and ring chromosomes as,
408
chromosome instability syndromes in,
412
sex chromosome aneuploidy in,
408-410,
409t
Klinefelter syndrome as,
410
Cytokines,
e117-1
in atopic dermatitis,
802
defective production of,
729
in
Mycoplasma pneumoniae,
1030
in neonatal immunity,
632
in systemic lupus erythematosus,
843
Cytokine receptor γ chain, mutations in gene encoding,
732,
732f
Cytomegalic inclusion disease,
1116
Cytomegalovirus (CMV),
1115-1117
following organ transplantation,
e171-2
immune globulin for,
882t
inflammatory bowel disease
versus,
1297,
1298t
maternal
fetal and neonatal effects of,
e89-3t
transfusion-associated,
e468-1
Cytomegalovirus immune globulin (CMV-IG),
e237-5
Cytopathic effect (CPE),
e164-4
Cytosolic acetoacetyl CoA thiolase deficiency,
434-435
Cytosolic 5’-nucleotidase, overactive,
e83-9
Cytotoxics
for juvenile idiopathic arthritis,
838t
Cytotoxic T cells
development and differentiation of,
e117-1
interaction with other immune cells,
e117-5
Cytotoxic T lymphocyte-associated 4 gene,
1971
D
Dacryocystitis,
2167t,
2183
with congenital nasolacrimal duct obstruction,
2165
Dance therapy for pain management,
371
D antigen, isoimmune hemolytic disease from,
615
Dapsone
for
Mycobacterium leprae,
e206-4
Daptomycin,
e173-14
for
Staphylococcus aureus,
907t
for vancomycin-resistant
Enterococcus,
e179-2
Datura stramonium toxicity,
269t
Daunorubicin for cancer therapy,
e488-4t
Davidenkow syndrome,
2138
Daydreaming, seizures and,
e587-5
Daytime frequency syndrome of childhood,
1851
Death,
1-2
due to acute rheumatic fever,
920
ethics in declaration of,
e3-3
leading causes of by age,
18f
due to maltreatment,
136t
of parent or sibling,
e16-2
of preterm and low birthweight infants,
563
due to undernutrition,
173
Death by neurologic criteria (DBNC),
e3-3
Death rate(s)
birthweight categories in,
e87-1f
from neonatal bacterial meningitis,
646
by sex, race, and, age,
3t
worldwide indicators of,
3t
Decimal factors, prefixes denoting,
e708-1t
Decision-making in palliative care,
153
Deep tendon reflexes assessment
in neurologic examination,
e584-7
Deep vein thrombosis (DVT),
1709
estrogen contraceptives and,
e548-3
Degenerative diseases, ataxia with,
2055
Dehydration
calculation of fluid deficit in,
246
clinical manifestations of,
246,
246t
laboratory findings in,
246
management of,
247,
247t
in protein-energy malnutrition,
178t
due to
Shigella infection,
960
symptoms associated with,
1333t
due to traveler’s diarrhea,
e168-5
Dehydroepiandrosterone (DHEA)
in ovarian carcinomas,
1872t
Dehydroepiandrosterone sulfate (DHEAS),
686
Deiodination defects,
1896
Déjerine-Sottas disease,
e605-1
Delayed eruption of teeth,
e13-4
Delayed sleep phase disorder (DSPD),
53-54
Del Castillo syndrome,
1945
Delirium
hypothyroidism-associated,
1903t
Delivery
birth injury due to
of spine and spinal cord,
573
cesarean section for,
e89-4
high-risk pregnancy and,
e89-4
Delivery room
care of newborn in,
536-538
antiseptic skin and cord care in,
537
maintenance of body heat in,
536-537
emergencies in,
575-579
abdominal wall defects as,
578
failure to initiate or sustain respiration as,
575
meconium staining as,
577
respiratory distress and failure as,
575
δ Fraction bilirubin,
1375
De Morsier syndrome,
2006
Demyelinating disorders of central nervous system,
2076-2080,
2076t
neuromyelitis optica as,
2077
stroke-like events
versus,
2085
Dengue shock syndrome,
1148
Dense body syndrome,
1722
Dental procedures, infective endocarditis prophylaxis for,
1626t
Dentatorubropallidoluysian atrophy,
2057t
Dent disease,
227,
1814
hypophosphatemia due to,
207
Dentin, injuries to,
1258t
Deoxyguanosine kinase (dGK),
1406
Dependence, chemical,
677
Depot medroxyprogesterone acetate (DMPA),
1875
Depression
attention deficit/hyperactivity disorder
versus,
110
maternal, child adjustment and,
e6-3f
psychopharmacologic management of,
61t,
63t
treatment of in palliative care,
157t,
158
in type 1 diabetes mellitus,
1986
Deprivation amblyopia,
2152
Dermacentor andersoni,
1041
Dermacentor variabilis,
1041
Dermatitis
atopic,
801-807
of external ear canal,
2199
laboratory findings in,
803
Hun T-lymphocyte-associated,
e269-1
Dermatomal distribution in herpes zoster,
1107,
1107f
Dermatomyositis
cardiac manifestations of,
1531t
Dermatophagoides farinae,
768
Dermatophagoides pteronyssinus,
768
Dermis
disorders of,
2273-2282
corticosteroid-induced atrophy as,
2274
Ehlers-Danlos syndrome as,
2278
elastosis perforans serpiginosa as,
2279,
2279f
focal hypoplasia as,
2222
reactive perforating collagenosis as,
2279,
2279f
Desensitization
systematic for phobias,
81
Desipramine
for attention deficit/hyperactivity disorder,
111t
for pain management,
364t
Desloratadine
for urticaria and angioedema,
815t
Desmoplastic small round cell tumor (DSRCT),
1773
Desmopressin acetate (DDAVP)
for central diabetes insipidus,
1883
for nocturnal incontinence,
1852
for platelet dysfunction,
1722
Desquamation in Kawasaki disease,
863,
864f
Deterministic effects of radiation,
2448
Detrusor-sphincter dyssynergia,
1849
Developmental delay,
39
in foreign-born adoptee,
131
in foster care children,
e35-2t
Developmental dysphasia,
117
Developmental dysplasia of hip (DDH),
2356
Developmental history in psychiatric diagnostic evaluation,
60
Developmental Milestones (DM),
41t-43t
Developmental plasticity,
e6-9
Developmental therapy for neurodevelopmental dysfunction,
e29-8
Dexamethasone
for bacterial meningitis,
2094
for chemotherapy-associated vomiting,
1244t
possible adverse reactions to in premature infant,
563t
Dexamethasone suppression test,
1940
Dextrose for oral hypoglycemic poisoning,
263
Diabetes, lipoatrophic,
1995
Diabetes mellitus (DM),
1968-1997
cystic fibrosis-related,
1996
genetic defects of insulin action in,
1995-1996
impaired glucose tolerance as,
1993
maternally inherited diabetes and deafness as,
1994-1995
necrobiosis lipoidica with,
2275
Diabetic ketoacidosis (DKA),
1976
Diabetic neuropathy,
1989
Diagnostic otoscope head,
2202
Dialectical behavior therapy (DBT),
95
Diamond-Blackfan anemia (DBA),
1650-1651
transient erythroblastopenia of childhood
versus,
1652t
Diaper changing in nursery,
538
Diarrhea,
1243-1245,
1245t See also Gastroenteritis See also Malabsorption
associated with hemolytic-uremic syndrome,
1791,
1791t
chloride-losing, congenital,
223
differential diagnosis of,
1246t
exclusion from day care due to,
e15-2t
hemolytic-uremic syndrome following,
1791,
1791t
in Kawasaki disease,
864f
metabolic acidosis due to,
232
nondigestive causes of,
1241t
Plesiomonas shigelloides,
e196-3
rotavirus, calcivirus, and astrovirus,
1134-1137
due to shellfish poisoning,
e703-5
treatment of in palliative care,
157t
watery
in microvillus inclusion disease,
1305
in tufting enteropathy,
1311
Diastolic overload pattern,
1539
Diastrophic dysplasia sulfate transporter (DTDST), loss of,
2430-2431
Diazepam
for muscle spasm in palliative care,
155t-156t
for spasticity of cerebral palsy,
2064
Dicarboxylic aminoaciduria,
1319
Diet
dental caries development and,
1256
for eosinophilic esophagitis,
1270
habits regarding in eating disorders,
92t
ketogenic for seizures,
2032
pesticide exposure through,
e700-2
Dietary fiber
for functional abdominal pain,
1348t
Dietary lipids, transport of,
471
Dietary supplements,
270-273,
271t-272t
nutritional aspects of,
169
Spanish-English botanical name translation chart,
274t
Diethylstilbestrol (DES)
uterine anomalies due to exposure to,
e548-3
Diffenbachia toxicity,
269t
Differential agglutination test, in toxoplasmosis,
1214
Diffuse cutaneous leishmaniasis (DCL),
1188
Diffusely adherent
Escherichia coli (DAEC),
964
Diffusing capacity for carbon monoxide (DLCO),
e366-3
Diffusion, pulmonary,
318
DiGeorge chromosomal region (DGCR),
728-729
congenital heart disease and,
e418-1
Digestive system disorders
anaerobic organisms in,
e205-1
cutaneous manifestations of,
e637-5
disorders of in mucopolysaccharidoses,
515t
of esophagus
eosinophilic esophagitis as,
1270
infective esophagitis as,
1270
obstructing and motility disorders as,
1263-1264
“pill” esophagitis as,
1270
of exocrine pancreas
associated with pancreatic insufficiency,
1369-1370
pancreatic function tests in,
e340-1
failure to thrive in,
148t
intestinal
eosinophilic gastroenteritis as,
1304
Meckel diverticulum and other remnants of omphalomesenteric duct as,
1281-1282,
1282f
pilonidal sinus and abscess as,
1362
rectal mucosal prolapse as,
1361
of liver and biliary system
of newborn,
600-612
jaundice and hyperbilirubinemia as,
603-608
meconium ileus in cystic fibrosis as,
601,
601f
meconium peritonitis as,
601
of oral cavity
associated with other conditions,
1251,
1251t
of salivary glands and jaw,
e308-1
of peritoneum
epigastric hernia as,
1418
in premature infants,
559t
psychopharmacology and,
65
signs and symptoms of
abdominal distention and abdominal masses,
1249
of stomach
eosinophilic gastroenteritis as,
1304
gastric duplication as,
1276
gastric volvulus as,
1276
hypertrophic gastropathy as,
1276
due to whole-body irradiation,
e699-4
Digestive system manifestations,
1241t
in chronic kidney disease,
1823t
in congenital disorders of glycosylation,
e81-7t
in factitious disorder by proxy,
146
in multiple organ dysfunction syndrome,
312t
in Neonatal Intensive Care Unit Neurobehavioral Scale,
624t
in systemic inflammatory response syndrome,
309t
Digit
centers of ossification appearance in,
29t
herpes simplex virus infection of,
1100,
1100f
Digital clubbing
nonpulmonary disease associated with,
e366-2t
Digitalis purpurea, potential toxicity of,
272t-273t
Digitus minimus varus,
2342
Dihydrolipoyl dehydrogenase deficiency,
431
Dihydropyrimidinase (DPH) deficiency,
e83-8
Dihydropyrimidine dehydrogenase (DPD) deficiency,
e83-8
1,25Dihydroxycholecalciferol
2D
3 (1,25(OH)
2D
3),
1922,
e694-1
Diltiazem for pulmonary hypertension,
1602t
Dilution therapy for internal radiation contamination,
e699-5
Dimenhydrinate for motion sickness,
1244t
Dimension of Quality,
e2-1
Dimercaprol
for arsenic and mercury intoxication,
e701-4
Dimercaptosuccinic acid (DMSA)
for arsenic and mercury intoxication,
e701-4
Dimercaptosuccinic acid (DMSA) renal scan,
1833,
1833f
Diphenhydramine
for cyclic vomiting syndrome,
1244t
Diphtheria acellular pertussis (DTaP) vaccine,
884t,
947-948,
993
with
Haemophilus influenzae type b vaccine (DTaP/Hib),
884t
hepatitis B-inactivated polio vaccine (DTaP-HepB-IPV),
884t
with inactivated polio vaccine and
Haemophilus influenzae type b vaccine (DTaP-IPV/Hib),
884t
with inactivated polio vaccine (DTaP-IPV),
884t
recommended schedule for,
886,
887f
Direct DNA-based mutation testing,
376,
377t
Direct fluorescent-antibody (DFA),
e164-1t
Disability in pediatric emergency assessment,
281
Disabled newborn, ethics in care of,
e3-2-e3-3
Disasters
natural, drowning during,
343
Discharge examination of newborn,
532
Discharge planning
for psychiatric hospitalization,
66
Discipline for preschoolers,
36
Discoid lateral meniscus (DLM),
2352
Discoid rash in systemic lupus erythematosus,
842,
842f
Discourse problems,
e29-2
Discreet Event Stimulation (DES),
e2-5f
Discrimination, chronic illness and,
e39-3
Disease detection in well child care,
14
Disease-modifying antirheumatic drugs (DMARDs)
for juvenile idiopathic arthritis,
837,
838t
Disease prevention in well child care,
14
Disequilibrium syndrome,
e52-2
Disimpaction, fecal,
74,
74t
Dislocation
hip, with arthrogryposis,
e674-4
Disorders of sex development (DSD),
1958-1968,
1960f
etiologic classification of,
1959t
undescended testis in,
1859
Dispatch center in transport medicine,
e61-7
Disposition in pharmacokinetics,
e57-2
Disruptive behavioral disorders,
96-100,
97t
in childhood and adolescence,
99-100
in infancy and toddlerhood,
99
Disseminated gonococcal infection (DGI),
937,
939
Disseminated tuberculosis,
998,
1004
Distal humeral fracture,
2392
Distal renal tubular acidosis,
208
Distention, abdominal,
1249
nondigestive causes of,
1241t
Distraction for pain management,
370-371
Distributive shock,
285,
307t
clinical manifestations of,
308
hemodynamic variables in,
311t
Diuretics
for acute renal failure,
1820
for hypertension
of chronic kidney disease,
1825
metabolic alkalosis due to,
236-237
Divalproex for mood stabilization,
64t
Dizziness in ear disorders,
e628-1
DNA
malignancy susceptibility associated with defects in repair of,
e486-1
messenger, in sudden infant death syndrome,
1427
DNA-based mutation testing, direct,
376,
377t
DNA markers in neuromuscular disorders,
2110
Dobutamine
for cardiac output maintenance and post-resuscitation stabilization,
294t
in neonatal resuscitation,
577
Docosahexaenoic acid (DHA),
e41-15
Doctrine of double effect (DDE),
e3-2
Documentation of female genital examination,
e542-2
Docusate for constipation in palliative care,
155t-156t
Doll’s eyes reflex, brain death and,
e63-2t
Dominant dystrophic epidermolysis bullosa (DDEB),
2246,
2246f
Donor
for heart transplantation,
e437-1
for intestinal transplantation,
e331-1
Do-not-attempt-resuscitation (DNAR) order,
153-154,
e3-2
Dopamine,
e568-1-e568-8,
e568-8f
for acute renal failure,
1820
for cardiac output maintenance and post-resuscitation stabilization,
294t
genetic disorders of,
445t
in neonatal resuscitation,
577
Dopamine antagonists for vomiting,
1244t
Dopamine β-hydroxylase deficiency,
421f,
446
Dopamine hypothesis in attention deficit/hyperactivity disorder,
e30-1
Dopamine 4 receptor gene,
108
Dopamine transfer gene,
108
Doppler echocardiography,
1542-1543,
1544f
in coarctation of the aorta,
1568
in ventricular septal defect,
1557
Dosages,
e57-9
chronic renal disease and,
e57-9
relationship between body weight, body surface and,
e708-11f
“Double bubble” sign in duodenal obstruction,
1278,
1278f
Double heterozygotes,
389
Double-inlet ventricle,
1592
Double-outlet right ventricle (DORV),
1582
with malposition of great arteries,
1588-1589
with pulmonary stenosis,
1588
Double quotidian fever,
e169-1
Down syndrome,
400-403,
401f
clinical features of,
402t
developmental milestones in,
402t
general anesthesia and,
e70-13
health supervision in,
403t
hypothyroidism with,
1901
intellectual function in,
403f
self-help skills and,
403t
Doxycycline,
e173-3,
e173-4t-e173-11t
for
Chlamydia trachomatis,
1036
for gonococcal disease,
939
for louse-borne typhus,
1048
for lymphogranuloma venereum,
1038
for nontuberculous mycobacteria,
e206-4
for Rocky Mountain spotted fever,
1043
for sexually transmitted infections in adolescents,
712t
Drag queens and kings,
655
Drowning,
341-348
as leading cause of death,
24
Drug(s)
adherence and compliance in,
e57-12
autoimmune hemolytic anemias due to,
1681,
1681t
diabetes mellitus associated with,
1986
dosages and regimens in,
e57-9
chronic renal disease and,
e57-9
dystonias induced by,
2059
for grief and loss,
e16-5
hypothyroidism due to,
1901
migraine secondary to overuse of,
2046
newborn brain injury due to,
568-569
for office emergencies,
e61-2t
for psychiatric disorders,
60-65
for respiratory distress syndrome,
586
surrogate endpoints and biomarkers in,
e57-9
Drug dosages,
e57-9
chronic renal disease and,
e57-9
Drug hypersensitivity syndrome (DHS),
827t
Drug-induced adrenocortical insufficiency,
1927
Drug-induced movement disorders (DIMD),
2059
Drug-induced precocious puberty,
1894
Drug-induced thrombocytopenia,
1718
Drug monitoring, therapeutic,
e56-1
Drug withdrawal, neonatal seizures due to,
2035
D-transposition of the great arteries (d-TGA),
1585,
1585f
Dual oxidase maturation factor 2 (DUOXA2),
e557-1
Duane retraction syndrome,
2006
Duchenne muscular dystrophy (DMD),
2119-2123
chronic severe respiratory insufficiency with,
1519
dilated cardiomyopathy with,
1630
laboratory findings in,
2120
Dulcolax for constipation in palliative care,
155t-156t
Duncan disease,
727
Epstein-Barr virus and,
1112
Dunnigan-type lipodystrophy,
2286
Dwarfism
cardiac manifestations of,
1531t
Dye studies in aspiration syndromes,
1472t
Dynamic compliance (C
DYN) assessment in mechanical ventilation,
328
Dysautonomia, familial,
2142
fever of unknown origin due to dysfunction of,
901
Dysbetalipoproteinemia, familial,
473t,
476
Dyschondrosteosis, Leri-Weil,
388-389
Dysentery
Plesiomonas shigelloides,
e196-3
Dysfluency (stuttering, stammering),
34,
122,
122t
Dysfunction Voiding Symptom Score,
1848,
1848f
Dyshidrotic pompholyx,
2253
Dyslipidemia
with type 2 diabetes mellitus,
1993t
Dysphasia, developmental,
117
Dysplasia,
e102-1t,
e664-1t,
e102-1-e102-2
focal facial ectodermal,
2222
intestinal epithelial,
1341
polyostotic fibrous, precocious puberty due to,
1892,
1892f
Schimke immunoosseous,
1690
septo-optic,
527
diabetes insipidus with,
1883
Dyspnea
as manifestation of extrapulmonary disease,
1526,
e413-1t
in palliative care,
157
nonpharmacologic treatment of,
157t
Dysthymic disorder,
87,
87t
Dystonia musculorum deformans,
2059
E
Eagle-Barrett syndrome,
1845
Ears
newborn assessment of,
534
Ear disorders
facial paralysis due to,
e628-1
hearing loss as,
2188-2196
genetic counseling in,
2196
incidence and prevalence of,
2188
in mucopolysaccharidoses,
515t
nontuberculous mycobacterial infection as,
1012t
otitis media as,
2199-2213
clinical manifestations of,
2202
developmental sequelae of,
2213
Haemophilus influenzae in,
943
Moraxella catarrhalis in,
e188-1
otitis media with effusion as
Toxoplasmosis gondii in,
1213
Early adolescence, growth and development during,
649-653,
650t
implications for pediatricians and parents,
653
relationships with family, peers, and society,
652-653
Early childhood, well child care in,
16
Early epileptic infantile encephalopathy (EEIE),
2023
Early exfoliation in dental development,
e13-4
Early myoclonic infantile encephalopathy (EMIE),
2023
Eating
foreign-born adoptees and,
131
Eating disorders,
90-96
definitions associated with,
90,
90t
differential diagnosis,
91
laboratory findings in,
91
Eaton-Lambert syndrome,
2133
Ecchymosis of eyelid,
2184
Eclampsia,
e89-2t
maternal diabetes mellitus and,
545
Ecologic model of development,
e6-2
Ectopic pancreatic rests,
1368
Ectopic undescended testis,
1859
Eczema
immunodeficiency with thrombocytopenia and,
734-735
Eczematous disorders,
2249-2254
of external ear canal,
2199
vesicular hand and foot dermatitis as,
2253,
2253f
Edema
cerebral
with fulminant hepatic failure,
1414
due to type 1 diabetes mellitus,
1981
laryngeal, in hereditary angioedema,
815
peripheral, physical examination of,
1531
Edematous malnutrition,
175
Edinburgh Postnatal Depression Scale,
e7-2t
Edrophonium chloride, in myasthenia gravis diagnosis,
2134
Education
children born to teen mothers and,
701
continuing, for emergency medical services for children,
e61-1
foster care children and,
e35-2t
for injury prevention,
20,
20t
in intellectual disability,
128
sex
for special needs girls,
1874
Educational diagnostician,
e29-7
Educational outreach in transport medicine,
e61-9
Edwardsiella tarda,
1298t
Effectiveness in quality of care,
e2-1
Efficiency in quality of care,
e2-1
Effusion
pericardial, tuberculous,
1009
Ehlers-Danlos syndrome (EDS),
1722,
2278
cardiac manifestations of,
1532t
Eicosapentaenoic acid (EPA),
e41-15
8 Millennium Development Goals (MDGs),
1,
173-174
Elastase
in chronic diarrhea,
1344t
Elastosis perforans serpiginosa (EPS),
2279,
2279f
Elbow
arthrogryposis involving,
e674-5
musculoskeletal pain syndrome of,
877t
Electrocardiography (ECG),
1537
in brain death diagnosis,
e63-3
in congenital hypothyroidism,
1900
in congenital intestinal pseudo-obstruction,
1283t
follow open heart surgery,
1604
in neuromuscular disorders,
2112
in pulmonary atresia,
1579
in pulmonary embolism,
1502
ST segment and T-wave abnormalities on,
1540,
1541f
in tetralogy of Fallot,
1575
twenty-four hour recordings in supraventricular tachycardia,
1614-1615
Electroencephalography (EEG)
in hypoxic-ischemic encephalopathy,
571,
571t
in intellectual disability,
127t
Electrolytes
absorption disorders of,
1319
measurement of in intravenous rehydration,
247
Electrolyte therapy for diarrheagenic
Escherichia coli,
964
Electromyography (EMG)
in juvenile dermatomyositis,
848
Electron transfer flavoprotein dehydrogenase (ETF-DH) deficiency,
461
Electron transfer flavoprotein (ETF) deficiency,
461
Electrophysiology studies,
e436-6
“Elephant ear” toxicity,
269t
Elimination half-life (T
1/2) of drug,
e57-2
Embryonal rhabdomyosarcoma,
1760
Embryonic development,
e6-7
Embryonic testicular regression syndrome,
1963
Emedastine difumarate for allergic conjunctivitis,
811t
Emergence from anesthesia,
e70-10
Emergency department (ED)
transport of child from,
278
visits by adolescents,
663
visits due to injury,
19,
19f
Emergency(ies),
279-296
airway management techniques for,
284-285
humanitarian, international rescues associated with,
e61-14t
neurologic,
e63-1-e63-3
abusive head trauma as,
301
hypoxic-ischemic insult and encephalopathy as,
301-303,
302f
intracerebral hemorrhage as,
303-304
status epilepticus as,
303
parenchymal lung disease as,
284
post-resuscitation care after,
296
secondary assessment in,
281
thoracentesis and chest tube placement for,
295
Emergency medical services for children (EMSC),
e61-1-e61-16
continuum of care model in,
e61-12
disaster preparedness in,
e61-5
provider capabilities in,
e61-3
role of primary care physician in,
e61-1
staff training and continuing education in,
e61-1
Emergency medical technicians (EMTs),
e61-3
Emergency Triage Assessment and Treatment (ETAT),
e61-15
Emery-Dreifuss muscular dystrophy,
2113t,
2123
Emotional development,
e6-3-e6-4
in foreign-born adoptees,
131
during middle childhood,
38
during preschool years,
35-36
Empirical use of antibacterial agents,
903
Enalapril
for systemic hypertension,
1645t
Enamel, injuries to,
1258t
Encephalitis
varicella-zoster virus,
1109
Encephalopathy(ies),
2061-2069
due to cat-scratch disease,
985
early epileptic infantile,
2023
early myoclonic infantile,
2023
hypertensive,
2068
strokelike events
versus,
2086
vaccine, febrile seizures with,
2017
Zellweger syndrome as,
2069
Encounters, cultural,
e4-4
Endocarditis
in acute rheumatic fever,
922
due to coagulase-negative staphylococci,
910
infective,
1622-1626
acute rheumatic fever
versus,
923,
923t
congenital heart disease and,
1609
prognosis and complications of,
1624
retinopathy associated with,
2180
in tetralogy of Fallot,
1576
Pseudomonas aeruginosa in,
976t
Staphylococcus aureus in,
905
Endochondral ossification,
e664-1
Endocrine disorders
of adrenal glands
congenital adrenal hyperplasia and related disorders as,
1930-1939
primary aldosteronism as,
e572-1
cardiac manifestations of,
1531t
failure to thrive in,
148t
gonadal
pseudoprecocity resulting from ovarian lesions as,
1957-1958
pseudoprecocity resulting from testicular tumors as,
e578-1
hypoglycemia associated with,
527-528
of hypothalamus and pituitary gland
hyperpituitarism, tall stature, and overgrowth syndromes as,
e554-1-e554-6
in myotonic muscular dystrophy,
2124
of parathyroid gland
pseudohypoparathyroidism (Albright hereditary osteodystrophy) as,
1919-1920
in premature infants,
559t
systemic inflammatory response syndrome and,
309t
of thyroid gland
thyroxine-binding globulin defects as,
e558-1
Endocrine factors in acute intermittent porphyrias,
e85-5
Endocrine system
chemical pollutants effect on,
e700-3
lysosomal storage disorders and,
485t
multiple organ dysfunction syndrome and,
312t
overweight and obesity and,
183,
183f
in physiology of puberty,
e555-1
Endodermal sinus tumor, vaginal,
1873
Endometrial stroma sarcoma,
1873
Endometrium, amenorrhea and,
688
Endophthalmitis,
2167t
Pseudomonas aeruginosa,
976t
Endoscopic repair of vesicoureteral reflux,
1837f,
1838
Endoscopic retrograde cholangiopancreatography (ERCP),
1379
Endoscopy
in cystic fibrosis treatment,
1493
in gastroesophageal reflux disease,
1267,
1268f
Endotoxin in
Neisseria meningitidis,
930
Endotracheal intubation
aspirate diagnostic microbiology,
e164-2
for asthma exacerbation,
800
complications of in newborn,
586-587
for congenital diaphragmatic hernia,
595
for infectious acute upper airway obstruction,
1448
manual ventilation before and after,
320-321
medications for placement of,
321t
for respiratory distress and failure,
320
size and depth dimensions for,
320t
Enema
for fecal disimpaction,
74t
Enlargement of cardiac chambers,
1537
ENPP1 gene mutation,
182t
Entamoebe histolytica rhomboid protease 1 (EhROM1),
1178-1179
Enteric adenoviruses,
1135
Enteric fever,
954-958
differential diagnosis of,
957
Enteric hyperoxaluria,
440
Enteric infection, chronic diarrhea due to,
1340
Enteroaggregative
Escherichia coli (EAEC),
962t,
963-964
Enterocolitis
food protein-induced,
821
Enterocolonic fistula with Crohn disease,
1300-1301
Enterocyte defects, chronic diarrhea due to,
1341
Enterocyte heparin sulfate deficiency,
1311
Enteroenteric fistula with Crohn disease,
1300-1301
Enteropathy
food protein-induced,
821
Enteroviruses,
1088-1094
complications and prognosis for,
1094
in type 1 diabetes mellitus development,
1971
in viral meningoencephalitis,
2095
Enthesitis-related arthritis (ERA),
e150-1-e150-3
in juvenile idiopathic arthritis,
831t
Envenomations,
2460-2465
hemolytic anemia secondary to,
e459-1
due to hymenoptera sting,
2464
due to scorpion sting,
2464
Environment
modification for injury prevention,
20,
20t
Environmental control measures
Environmental exposures in childhood cancers,
1725
Environmental factors
in acute lymphocytic leukemia,
1732t
in childhood injuries,
21
in inflammatory bowel disease,
1295
in overweight and obesity,
182
in psychosomatic illness,
67-68
in systemic lupus erythematosus,
841
in type 2 diabetes mellitus,
1991
Environmental health hazards
envenomations as,
2460-2465
due to hymenoptera sting,
2464
due to scorpion sting,
2464
Enzymes
muscle-derived in juvenile dermatomyositis,
848,
848t
serum in neuromuscular disorders,
2110
Enzyme deficiencies
pancreatic,
1369
cystic fibrosis and,
1495
Enzyme-linked immunofiltration test (ELIFA),
1214
Enzyme-linked immunosorbent assay (ELISA)
in arboviral encephalitis,
1144
in
Clostridium difficile infection,
995
in coccidioidomycosis,
1066
Enzyme-linked immunospot (ELISPOT) assay,
e164-4
Enzyme-linked immunotransfer blot (EITB),
1235
Enzyme multiplicity,
e56-4
Enzyme replacement therapy (ERT)
for genetic disorders,
380
for mucopolysaccharidoses,
514
Eosinophil cationic protein (ECP),
739
Eosinophil count,
739-740
in immigrant children,
133
Eosinophilia
allergic disease and,
740,
766
infectious disease and,
740
pulmonary infiltrates with,
1474
in strongyloidiasis,
1223
Eosinophilic cystitis,
1830
Eosinophilic esophagitis (EoE),
1264,
1270
Eosinophilic gastroenteritis,
1304
Eosinophilic pustular folliculitis (EPF),
2220
Ephedra alkaloids for performance enhancement,
2423t
Ephedrine
adolescent abuse of,
675t
for myasthenia gravis,
2135t
Ephelides (freckles),
2236
Epicondylitis, lateral,
2411
Epidemic dengue-like disease,
1147
Epidemic keratoconjunctivitis,
2168
Epidermal inclusion cyst,
2328
Epidermal nevus syndrome,
207
Epidermodysplasia verruciformis,
2315f
Epidermolysis bullosa simplex (EBS),
2244,
2245f
Epidural abscess, poliovirus infection
versus,
1085t
Epidural hemorrhage in newborn,
566
Epilepsia partialis continua,
2019
Epileptic encephalopathy,
2013
Epileptic syndrome,
2013
with generally good prognosis,
2016t
Epimastigotes, in trypanosomiasis,
1193,
1193f
Epimerase deficiency,
503
Epinastine hydrochloride,
811t
Epinephrine,
e568-1-e568-8,
e568-8f
for cardiac output maintenance and post-resuscitation stabilization,
294t
hypoglycemia due to deficiency of,
528
for pediatric resuscitation and arrhythmias,
294t
in pheochromocytoma,
1942
Epiphyseal dysplasias, multiple,
2427
Epithelial cancer
incidence and survival rates for,
1726t
Epithelial cells
Chlamydophila pneumoniae in,
1034f
Epstein-Barr virus in,
1111
Shigella invasion of,
959
Epithelial dysplasia, intestinal,
1341
Epithelioma, basal cell,
e662-3
Epoprostenol for pulmonary hypertension,
1602t
Epstein-Barr virus (EBV),
1110-1115
Hodgkin lymphoma and,
1740
maternal
fetal and neonatal effects of,
e89-3t
predisposition to infection due to immunodeficiency,
716t
after transplantation,
e171-2
hematopoietic stem cell transplantation,
763
Equal pressure point (EPP),
1420
Equipment
in international pediatric emergency medicine,
e61-15
Equity in quality of care,
e2-1
Erosion, examination of,
e637-1
Erysipelas, group A streptococcus in,
917
Erythema
palmar, as manifestation of liver disease,
1376
Erythema nodosum leprosum (ENL) reactions,
e208-3
Erythematous rash of scarlet fever,
916f
Erythroblastosis fetalis,
615-619,
620t
due to ABO incompatibility,
619
Erythrocyte protoporphyrin (EP),
2450
Erythrocyte sedimentation rate (ESR)
in fever of unknown origin,
901
in immunodeficiency screening,
718t
Erythrogenic toxin in scarlet fever,
916
Erythrokeratoderma, symmetric progressive,
2270-2271
Erythrokeratoderma variabillis (EKV),
2270,
2271f
Erythromycin,
e173-3,
e173-4t-e173-11t
for
Chlamydophila pneumoniae,
1035
for cystic fibrosis lung infection,
1492t
for infectious diarrhea,
1337t
for
Legionella infection,
e200-2
for lymphogranuloma venereum,
1038
for neonatal infection,
645t
possible adverse reactions to in premature infant,
563t
for vulvovaginitis,
1868t
Erythropoietic porphyria, congenital,
2256,
2256f
Erythropoietin (EPO)
in physiologic anemia of infancy,
1654
Escherichia coli,
961-965,
962t
hemolytic-uremic syndrome following,
1791
maternal
fetal and neonatal effects of,
e89-3t
Shiga toxin-producing,
963
in traveler’s diarrhea,
1338t
Escherichia coli 0157:H7
in diarrhea-associated hemolytic-uremic syndrome,
1791-1792
inflammatory bowel disease
versus,
1298t
Esophageal bleeding,
1261
Esophageal pH monitoring,
1472t
Esophagitis
due to gastroesophageal reflux disease,
1269
Esophagus
disorders of
eosinophilic esophagitis as,
1270
infective esophagitis as,
1270
laryngotracheoesophageal clefts as,
1263
obstructing and motility disorders as,
1263-1264
“pill” esophagitis as,
1270
mega-, in Chagas disease,
1196
Essential fatty acid deficiency,
e41-15
Essential pentosuria,
e81-5
Estimated energy requirement (EER),
e41-4
equations for,
e41-1t
physical activity coefficients for,
e41-1t
Estradiol in ovarian carcinomas,
1872t
Estrogens
gynecomastia due to exogenous sources of,
1950
for overgrowth syndrome,
e554-2
porphyria cutanea tarda and,
e85-11
for Turner syndrome,
1954
vaginal bleeding due to exposure to,
1870
Estrogen contraceptives
for special needs girls,
1875
E
3 subunit deficiency,
431
Etanercept
for juvenile idiopathic arthritis,
838t
Ethics/ethical factors,
e3-1-e3-8
assent and parenteral permission in,
e3-1
in balancing maternal and fetal interests,
e3-6
consultations regarding,
e3-4
in long-term mechanical ventilation,
330-331
in newborn screening and genetic testing,
382-383,
e3-4
in religious or cultural objections to treatment,
e3-3-e3-4
in treatment of critically ill children,
e3-1-e3-2
Ethylene glycol poisoning,
267-268
metabolic acidosis due to,
233
Etoposide for cancer therapy,
e488-4t
Europe, pediatricians per population in,
12f
European hornet, allergic responses to,
807f
European immunization schedule,
895
Eustachian tube anatomy, otitis media and,
2201
Eutectic mixture of local anesthetics (EMLA),
367
Euvolemic hyponatremia,
216
Evaporation heat loss in newborn,
536-537
Eventration of diaphragm,
597
Evidence-based practice,
16
Excessive daytime sleepiness (EDS),
53
Exchange programs, international,
e61-16
Exchange transfusion
for erythroblastosis fetalis,
618
Excimer laser correction for myopia,
2151
Excitability in seizures,
2025
Excoriation, examination of,
e637-1
Executive functioning (EF),
e29-4
Exercise
habits regarding in eating disorders,
92t
hematuria due to vigorous,
1799
hyperinsulinemia induced by,
527
Exercise challenge in asthma,
784,
785t
Exercise electrocardiography,
1545
Exercise-induced anaphylaxis,
814
Exercise-induced bronchospasm,
784
Exercise intolerance, as manifestation of extrapulmonary disease,
1526,
e413-1t
Exercise testing
in cardiovascular disease,
1545
in respiratory disease,
e366-4
Exercise therapy, graded, for chronic fatigue syndrome,
e115-3
Exhaled nitric oxide in asthma,
784-785
Exhaled tidal volume (VTE),
328
Exocrine pancreas
disorders of
associated with pancreatic insufficiency,
1369-1370
pancreatic function tests in,
e340-1
Exoerythrocytic phase of malaria,
1199,
1199f
Exopolysaccaride biofilm of coagulase-negative staphylococci,
909
Expansile skeletal hyperplasia,
e697-1
Expedited partner therapy (EPT),
714
Experimental strategies in Marfan syndrome,
2445
Expiratory time constant in mechanical ventilation,
323
Expiratory time in mechanical ventilation,
327
Exposure
in pediatric emergency assessment,
281
Extensively drug resistant (XDR),
1009
External auditory canal
congenital stenosis or atresia of,
e630-1
External ear, malformations of,
e630-1
External jugular vein, venous access in,
295f
External tibial torsion,
2347
Extracorporeal membrane oxygenation (ECMO)
for congenital diaphragmatic hernia,
595-596
for persistent pulmonary hypertension of the newborn,
593-594
Extrahepatic cholestasis,
1381
Extraocular muscles
congenital fibrosis of,
2006
weakness of in neuromuscular disorders,
2115t
Extrapulmonary sequestration,
1466
Extravascular drug absorption,
e57-5
Extremity(ies)
conditions causing arthritic pain in,
836t
effects of eating disorders on,
93t
fracture of as birth injury,
579
fracture of as delivery room emergency,
579
newborn assessment of,
536
Extrinsic alveolar alveolitis,
1059
Extrusion injury, dental,
1259
Ex utero intrapartum treatment (EXIT) procedure,
577,
578f
Eye(s)
growth and development of,
e610-1
newborn assessment of,
534
Eye disorders
infection as
Cryptococcus neoformans,
1057
Haemophilus influenzae,
942
herpes simplex virus,
1101
newborn prophylaxis against,
537
of movement and alignment,
2157-2162
congenital ocular motor apraxia as,
2161
in mucopolysaccharidoses,
515t
optic neuropathy, leber hereditary as,
2067
of retina and vitreous,
2174-2181
Best vitelliform degeneration as,
2178
with blood disorders,
2180
coloboma of the fundus as,
2181
familial exudative vitreoretinopathy as,
2179
myelinated nerve fibers as,
2181
persistent fetal vasculature as,
2176
retinal detachment as,
2179
Stargardt disease as,
2178
with subacute bacterial endocarditis,
2180
Eyegrounds examination,
2016
Eyelid
ecchymosis and swelling of,
2184
Eye manifestations
in childhood cancers,
1728
in mitochondrial encephalomyopathy,
2065t
in systemic lupus erythematosus,
843t
F
Face
effects of malnutrition on,
175t
newborn assessment of,
534t
Facial ectodermal dysplasia,
2222
Facial nerve
neurologic examination of,
e584-5
Facial phenotype in congenital central hypoventilation syndrome,
1521
Facial weakness
in myotonic muscular dystrophy,
2123f
in neuromuscular disorders,
2115t
Facioscapulohumeral muscular dystrophy,
2113t,
2126
Factitial panniculitis,
2285
Factitious disorder,
69,
69t
Factitious disorder by proxy (FDP),
146-147
Factor I deficiency,
1704
Factor II
reference values for,
1698t
Factor V
deficiency of,
1703-1704
factor VIII deficiency combined with,
1704
reference values for,
1698t
Factor VII
reference values for,
1698t
Factor VIII
increased concentrations of,
1708
Factor X
reference values for,
1698t
Factor XI
reference values for,
1698t
Factor XII
reference values for,
1698t
Factor XIII
reference values for,
1698t
Facultative anaerobes,
995
Failure to thrive (FTT),
147-149
clinical manifestations of,
147
growth charts in assessment of,
e13-3
Fairbanks apprehension sign,
2355
Familial aplastic anemia,
1690
Familial apolipoprotein A-1 deficiency,
477
Familial clustering, genetic,
389-390
Familial cold autoinflammatory syndrome (FCAS),
814,
855t,
858
Familial combined hyperlipidemia (FCHL),
473t,
475
Familial defective APOB-100 (FDB),
473t,
475
Familial dysalbuminemic hyperthyroxinemia,
e558-1
Familial dysautonomia,
2142
fever of unknown origin due to dysfunction of,
901
Familial dysbetalipoproteinemia (FDBL),
473t,
476
Familial exudative vitreoretinopathy (FEVR),
2179
Familial glucocorticoid deficiency,
1924-1925
Familial hemiplegic migraine,
e587-2
Familial hemophagocytic lymphohistiocytoses (FHLH),
1774-1776
Familial Hibernian fever,
858
Familial hypercalciuric hypercalcemia,
1922-1923
Familial hypercholanemia (FHC),
1384
Familial hypobetalipoproteinemia,
478
Familial lecithin-cholesterol acyltransferase (LCAT) deficiency,
477
Familial male gonadotropin-independent precocious puberty,
1893
Familial nonhemolytic unconjugated hyperbilirubinemia,
1389-1390
Familial peeling skin,
2268t
Familial protein intolerance,
455
Familial rectal pain syndrome,
e587-3
Family
communication with in post-resuscitation care,
296
discussion of cancer treatment with,
e488-3
impact of chronic illness on,
e39-2
obesity prevention in,
187t
well child care and,
16-17
Family-centered care
of foster care children,
e35-2t
Family child-care home,
895
Family counseling
in intellectual disability management,
129
in neurodevelopmental dysfunction,
e29-8
for psychiatric disorders,
66
Family factors in psychosomatic illness,
68
Family history
as cancer risk factor,
1727t
of cardiovascular disease,
1530
in genetic transmission,
383
in neurologic evaluation,
e584-1
in persistent hyperinsulinemic hypoglycemia,
522t
of type 2 diabetes mellitus,
1991
Family Psychosocial Screening (FPS),
41t-43t
Family systems, development and,
e6-2
Famotidine
for functional abdominal pain,
1348t
for
Helicobacter pylori gastritis,
1293t
for urticaria and angioedema,
815t
Fasciculation of muscle,
2109
Fasciitis, necrotizing,
2301-2302
group A streptococcal,
919
Fasting glucose
in impaired glucose tolerance,
e583-2t
Fasting time to hypoglycemia,
521t
Fat(s)
See also Lipids
adequate macronutrient distribution range for,
e41-1t,
e41-4
intake in type 1 diabetes mellitus,
1982,
1982t
Fatty acids
free, neonatal transient hypoglycemia and,
520-521,
522t
metabolic disorders of,
417t
Fatty liver
with type 2 diabetes mellitus,
1993t
Fear of self-injecting (FSI),
1986
Feasibility in quality measurement,
e2-2t
Febrile status epilepticus,
2017
Febrile ulcerative acne,
2328
Fecal incontinence,
73-74
Fecal leukocytes in chronic diarrhea,
1344t
Fecal occult blood in chronic diarrhea,
1344t
Fecal reducing substances in chronic diarrhea,
1344t
Fecal testing for parasitic infection,
e164-4
Federal funding for health care,
10
Feeding
with cleft lip or palate,
1252
cultural considerations in,
167-168
emotional development and,
27-28
enteral, for acute gastroenteritis,
1334-1336
failure to in newborn,
e92-2
during first year of life
of foreign-born adoptees,
131
of premature and low birthweight infants,
560-562,
561f
sudden infant death syndrome and care practices and exposures in,
1425
of toddlers and preschool-age children,
165,
165t
Felbamate
adverse effects of,
2031t
Femoral anteversion,
2346
Femoral neck
normal development of,
2344
Femoral torsion, internal,
2347
Femoral vein, venous access in,
292,
295f
Fentanyl
equianalgesic doses and half-life of,
367t
for pain management,
365t
possible adverse reactions to in premature infant,
563t
transdermal patch for pain management,
155t-156t
Ferritin
in congenital dyserythropoietic anemia,
e446-1t
in iron deficiency-anemia,
1656t
in systemic-onset juvenile idiopathic arthritis,
836
Ferrochelatase (FETCH),
e85-2f
Ferrous sulfate for restless leg syndrome,
52
Fertility
female, impact of cancer therapy on,
1870-1871
male, inguinal hernia repair and,
1368
Fetal aspiration syndrome,
590,
591f
Fetal breathing movements (FBMs),
543t
Fetal heart rate
in biophysical profile,
543t
Fetal hemoglobin (Hbf),
e440-5
syndromes of hereditary persistence of,
1673-1674
Fetal hydantoin syndrome,
2007t
Fetal thyroid hormones,
e557-2
Fetal tissue analysis,
543t
Fetal transfusion syndrome,
554
α-Fetoprotein concentration,
543t
in germ cell tumors,
1770
in ovarian carcinomas,
1872t
Fetus,
541-552
assessment of anatomy of,
549f
cardiac catheterization, interventional in,
1548
ethical considerations in balancing maternal interests and interests of,
e3-6
infections associated with,
543t,
547-548
congenital lymphocytic choriomeningitis,
548
maternal disease and,
545
radiation exposure to,
548
Fever(s),
e169-1-e169-3
in acute rheumatic fever,
922
in bacterial meningitis,
2094
in dengue-like disease,
1148
exclusion from day care due to,
e15-2t
home remedies among African Americans for,
e4-2t
with hyperimmunoglobulinemia D,
436
maintenance water and electrolytes and,
244
in returning travelers,
e168-7
in Rocky Mountain spotted fever,
1042
in systemic-onset juvenile idiopathic arthritis,
832-834,
834f
Fever of unknown origin (FUO),
898-902
in HIV, diseases associated with,
e171-4t
Fever syndromes, hereditary,
855-860,
855t-856t
chronic infantile neurologic cutaneous and articular disease as,
858
familial cold autoinflammatory syndrome as,
858
hyperimmunoglobulinemia D syndrome as,
857-858
Muckle-Wells syndrome as,
858
periodic fever, aphthous stomatitis, pharyngitis, and adenitis as,
859-860
pyogenic arthritis, pyoderma gangrenosum, and acne syndrome as,
858-859
tumor necrosis factor receptor-associated periodic syndrome as,
858,
859f
Fexofenadine
for urticaria and angioedema,
815t
Fiber, dietary
for functional abdominal pain,
1348t
Fibrillary infiltrating astrocytoma,
1748-1749
Fibrillin-1, abnormal biosynthesis of,
2440
Fibrinolytic system, tests of,
1699
Fibrinopurulent stage of empyema,
1507
Fibrin-stabilizing factor,
1696t
Fibroblast growth factor receptor (FGFR) mutations,
2013
Fibula
congenital and angular deformities of,
2350-2351
Fictitious hyperkalemia,
219
50% inhibitory dose (ID
50),
1069
Filament hemagglutinin (FHA),
944-945
Filamins, disorders involving,
2435
Financial costs
See Costs
Fine motor development,
e29-1
during first 2 years,
27t
Fire ant, allergic responses to,
807f
Fireworks-related injury,
23
First aid measures for burn injury,
350
First-degree heart block,
1618
electrocardiography of,
1540
First-degree relative,
383
First-generation antihistamines,
771,
771t
First heart sound, auscultation of,
1533
First-pass effect of drug,
e57-2
Fish tank granuloma,
1013
Fistula
rectobulbarurethral,
1357
rectoprostaticurethral,
1357
Five-year survival rates for cancer,
1726f
Flame-retardant sleepwear,
23
“Flesh-eating bacteria”,
e205-1
Flow cytometry
in B cell deficiency screening,
720
in leukocyte adhesion deficiency,
744
in T cell deficiency screening,
720-722
in X-linked agammaglobulinemia,
724
Flow study, antegrade pressure-perfusion,
1841
Flow volume loop
in intrapulmonary airway obstruction,
e365-3f
Fluconazole,
e225-1t,
e225-2
for coccidioidomycosis,
1067
for
Cryptococcus neoformans,
1058
for neonatal infection,
644
for
Paracoccidioides brasiliensis,
e233-1
Fluid intake
for premature and low birthweight infants,
559-560
Fluid management in kidney transplantation,
e530-5
Fluid replacement, intraoperative,
e70-9t
Fluid therapy,
242,
242t
for bacterial meningitis,
2094
for diarrheagenic
Escherichia coli,
964
intravenous solutions for,
243,
243t
selection of solutions for,
243
Flunarizine for migraine prophylaxis,
2044,
2044t
Flunitrazepam, adolescent abuse of,
675t
Fluorescent treponemal antibody absorption (FTA-ABS) test,
1019-1020
Fluoroquinolones,
e206-3
for
Staphylococcus aureus,
907t
Fluoroscopy
in respiratory disease diagnosis,
e366-2
Fluoxetine
for depression and anxiety symptoms,
63t
for pain management,
364t
for weight loss in adults,
187t
Flutter-like oscillations of eye,
2162
Focal cerebral arteriopathy (FCA),
2080
Focal cortical dysplasia,
2004
Focal dermal hypoplasia,
2222
Focal facial ectodermal dysplasia,
2222
Focal segmental glomerulosclerosis (FSGS),
1803t,
1804
renal transplantation in,
e530-2
Focused assessment with sonography in trauma (FAST),
339
Folate receptors, autoantibody against, maternal,
e89-2t
Folic acid,
194t
supplementation during pregnancy,
2001
supplementation for neural tube defect prevention,
552
Folinic acid as poisoning antidote,
258t
Follicle-stimulating hormone (FSH),
e550-2
Follicular bronchitis,
1463
Follicular conjunctivitis in
Chlamydia trachomatis,
1035
Follicular dendritic cells (FDCs),
e117-5
Follistatin in testicular function,
e576-4
Fontanels
in neurologic examination,
e584-2
Food and Agriculture Organization (FAO),
171
Food and Drug Administration (FDA),
547
Food assistance programs,
170
Food-borne illness
Staphylococcus aureus in,
906
Food challenges in allergic disease,
768
Foot
musculoskeletal pain syndrome of,
877t
painful, differential diagnosis for,
2344t
vesicular dermatitis of,
2253
Foot disorders
calcaneovalgus feet as,
2336
hypermobile pes planus (flatfoot) as,
2338,
2338f
talipes equinovarus (clubfoot) as,
2336,
2337f
Foramen of Morgagni hernia,
597,
597f
Forced expiratory volume in 1 sec (FEV
1),
1419
in pulmonary function testing,
e366-3
Forced expiratory volume in 1 sec (FEV
1)/forced vital capacity (FVC) ratio,
1419
Forced vital capacity (FVC)
in pulmonary function testing,
e366-3
Forensic evidence collection following rape,
704
Formeterol for asthma,
794t
Fosinopril for systemic hypertension,
1645t
Fosphenytoin
for neonatal seizures,
2037
Foster Care Independence Act of 1999,
e35-1
Fostering Connections to Success and Increasing Adoptions Act,
e35-1
Fourth Geneva Convention,
e36-6
Fourth heart sound, auscultation of,
1533
Fox-Fordyce disease,
2288
Fraction of inspired oxygen (FIO
2)
in mechanical ventilation,
327
oxygen administration and,
319
partial pressure of carbon dioxide divided into,
319
Fracture(s),
2387-2394,
2388f
of nose, as delivery room emergency,
579
timetable of radiologic changes in,
139t
Frameshift, genetic,
e74-2
Framework for well child care,
16
Franceschetti syndrome,
1254
Free water clearance, hyponatremia due to decreased,
1885
French-American-British (FAB) classification
of acute lymphocytic leukemia,
1732
Frenulum, lingual, short,
1240
Friedreich ataxia,
2055
cardiac manifestations of,
1531t
Frontal plagiocephaly,
2012
Fructokinase deficiency,
503
Fructose-1,6-diphosphatase deficiency,
524t,
529
Fukuyama congenital muscular dystrophy,
2127
Functional magnetic resonance imaging (fMRI),
e584-11
Functional residual capacity (FRC),
1419,
e365-2f
chest wall compliance and,
e365-2
in mechanical ventilation,
322,
323f
Fundoplication
for gastroesophageal reflux disease,
1268-1269
Fundus flavimaculatus,
2178
Fungal infections
fever of unknown origin in,
900t
following organ transplantation,
e171-8
predisposition to due to immunodeficiency,
716t
due to
Sporothrix schenckii,
e234-1
Fungi
rapid antigen detection of,
e164-1
Furosemide
for acute renal failure,
1820
for hypertensive emergencies,
1646t
for nephrotic syndrome,
1805
possible adverse reactions to in premature infant,
563t
for subcutaneous fat necrosis,
2284
for systemic hypertension,
1645t
Fusion genes, cancer associated with,
e486-1
Fusobacterium necrophorum,
e205-1
Fusospirochetal gingivitis,
2299
Futility, life-sustaining medical treatment and,
e3-1
G
Gabapentin
adverse effects of,
2031t
for migraine prophylaxis,
2044t
for neuroirritability in palliative care,
155t-156t
Gain-of-function gene mutation,
e74-3
Gait
of Legg-Calvé-Perthes disease,
2361
neurologic examination of,
e584-9
Gait, arms, legs, spine screen (GALS),
e664-2
Galactokinase deficiency,
502
Galactosemia,
524t
ovarian damage due to,
1956
Ganglioneuroblastoma, diarrhea caused by,
e333-2t
Ganglioneuroma, diarrhea caused by,
e333-2t
Gasping, sudden infant death syndrome and,
1428
Gastric content aspiration,
1470
Gastric duplication,
1276
Gastric fluid, loss of,
245
Gastric lavage for poisoning,
255-257
Gastric mucosa,
e320-1
malabsorption due to defects of,
1305t
Gastrin in neuroendocrine tumor-associated diarrhea,
e333-2t
Gastrinoma, diarrhea caused by,
e333-2t
Gastroesophageal junction (GEJ),
e310-1
Gastroesophageal reflux disease (GERD),
1266-1270
bronchopulmonary dysplasia with,
e410-1
clinical manifestations of,
1267
due to congenital diaphragmatic hernia,
596
epidemiology and natural history of,
1266
reactive airway disease,
1263
respiratory signs and symptoms of,
e413-1t
Gastrointestinal decontamination for poisoning,
255
Gastrointestinal obstruction
Gastrointestinal stromal cell tumor (GIST),
e337-3
Gastropathy, hypertrophic,
1276
Gastrostomy feeding of premature infant,
560
Gell and Coombs classification,
824
Gender factors
in childhood injuries,
20
Gender identity disorder,
656,
657t
Gene(s)
fusion, cancer associated with,
e486-1
Gene polymorphism
effects on drug response,
e56-2t
General appearance
in pediatric emergency assessment,
279
General assessment in pediatric emergency,
279,
280f
Generalized anxiety disorder (GAD),
80,
80t
Generalized epilepsy with febrile seizures plus (GEFS+),
2017
Generalized lipodystrophy,
2286
Generalized motor seizure,
2023
Gene-replacement therapies,
381
Genetic approach in pediatric medicine,
380-383
Genetic association,
e77-3
Genetic counseling,
377-379,
378t
in acute intermittent porphyrias,
e85-8
in chronic granulomatous disease,
746
in congenital heart disease,
e418-3
in erythropoietic protoporphyria,
e85-17
in neurofibromatosis,
2048
in peroxisomal disorders,
467
in transmissible spongiform encephalopathies,
e270-4t
in X-linked adrenoleukodystrophy,
470
Genetic disorders
diabetes mellitus associated with,
1986
failure to thrive in,
148t
genotype-phenotype correlations in,
e74-4
hypomelanosis of Ito,
412
Klinefelter syndrome as,
410
management and treatment of,
379-380
Pallister-Killian syndrome as,
412
severe intellectual disability in,
123t
Genetic epidemiology,
e77-1
Genetic factors
in childhood cancers,
1727t
in febrile seizures,
2017
in high-risk pregnancy,
e89-1
in psychosomatic illness,
68
Genetic heterogeneity,
376
Genetics
of antibody deficiency disorders,
723t
of attention deficit/hyperactivity disorder,
108
of autistic disorder,
102
of Chédiak-Higashi syndrome,
744
of chronic granulomatous disease,
745-746
of combined immunodeficiency disorders,
731t
of congenital central hypoventilation syndrome,
1520-1521
of congenital diarrheal disease,
1342t
of congenital muscle fiber-type disproportion,
2116
of craniosynostosis,
2012t
of febrile seizures,
2017
of hemolytic-uremic syndrome,
1792t
of hereditary spherocytosis,
1659t
of 21-hydroxylase deficiency,
1930
of hyperphenylalaninemia,
418
of hypopigmentation,
2238t
internet reference sites associated with,
380t
of language and communication disorders,
116
of leukocyte adhesion deficiency as,
741
of maple syrup urine disease,
431
of multiple pituitary hormone deficiency,
1876-1878
of myeloperoxidase deficiency,
745
of myotonic muscular dystrophy,
2123f
of myotubular myopathy,
2115
of nemaline rod myopathy,
2117
of nephrotic syndrome,
1803t
of neuromuscular disorders,
2110
of spinal muscular atrophy,
2137
types of professions associated with,
382,
382t
of von Willebrand disease,
1706
of Wiskott-Aldrich syndrome,
734
Genetic testing
in intellectual disability,
125,
127t
Genetic transmission,
383-394
multifactorial and polygenic inheritance in,
393-394,
393f
pseudogenetic inheritance and familial clustering in,
389-390
Genitalia
newborn assessment of,
536
preschooler curiosity regarding,
35
Genital tuberculosis,
1007
Genital ulcer syndromes,
708
Genitourinary disorders
anaerobic infection as,
e205-1
Chlamydia trachomatis infection as,
1035-1036
due to cystic fibrosis,
1487
due to typhoid fever,
957t
Genitourinary system of newborn,
e98-1
Genotype/genotyping
of acute lymphocytic leukemia,
1733f
Genotype-phenotype correlations in genetic disorders,
e74-4
Gentamicin,
e173-3,
e173-4t-e173-11t
for bacterial meningitis,
2093t
for gonococcal disease,
939
for infective endocarditis,
1625t
possible adverse reactions to in premature infant,
563t
for
Staphylococcus aureus,
907t
Geographic factors
in dengue-like disease,
1147t
in developmental dysplasia of the hip,
2356
in porphyria cutanea tarda,
e85-10
in worldwide death rates,
3-4,
3t
German chamomile for sedation,
271t
Germ line stat 1 mutation,
735
Germ tube test in candidiasis,
1053
Gestational age
eye examination schedule based on,
2175t
Ghon complex in tuberculosis,
998
Giant cells, in response to hepatic injury,
1394
Giant cell arteritis,
868t
Giant cell granuloma of jaw,
e308-1
Giant cell pneumonia,
1071
Giant papillary conjunctivitis,
810
Giggle incontinence,
1851
Gingival cysts of newborn,
2298
Gingival lesions, due to vitamin C deficiency,
198,
199f
Gingival overgrowth, cyclosporine- or phenytoin-induced,
1257
Ginkgo biloba for asthma,
271t
Girls
first sign of puberty in,
649
Gla-containing proteins,
210
Glandular disease,
Francisella tularensis,
979
Glasgow Coma Scale (GCS)
in traumatic brain injury,
298,
337
Glenn cavopulmonary anastomosis,
e426-3
Glenn shunt, bidirectional,
1581
Glenoid labrum tear,
2410
Gliding undescended testis,
1859
Glioma
environmental carcinogens and,
e700-3
Global abuse and neglect,
136
Global childhood injuries,
19
Global developmental delay,
124
Global hypoxic-ischemic insult,
301-303
Globulins
serum, liver disease and,
1378
Glomerular basement membrane (GBM),
e502-1
Glomerular tubular balance,
e52-5
Glomerulosclerosis, focal segmental,
1803t,
1804
Glossitis
due to riboflavin deficiency,
193f
Glossopharyngeal nerve, neurologic examination of,
e584-5
Glucocorticoids
for allergic disease,
772
receptor gene mutation,
1962
Glucocorticoid-remediable aldosteronism,
236
Glucocorticoid-suppressible hyperaldosteronism,
1938-1939
Glucocorticosteroids, topical,
2217t
Gluconeogenesis, disorders of,
504,
529
Glucose
See also Hyperglycemia See also Hypoglycemia
homeostasis of
in infants and children,
518
levels of in hyperinsulinism,
521t
in maintenance fluid therapy,
243
for pediatric resuscitation and arrhythmias,
294t
in plasma osmolality,
e52-2
as poisoning antidote,
258t
Glucose intolerance in chronic kidney disease,
1823t
Glucose-6-phosphatase dehydrogenase (G6PD)
Glucose tolerance test,
1993
Glucose transporter 1 (GLUT-1) defects,
529
Glucose transporter 2 (GLUT-2) defects,
499,
529
α-Glucosidase inhibitors,
1992t
Glucuronosyl transferase (UGT)
drug biotransformation and,
e56-8
Glutamate pyruvate in liver dysfunction evaluation,
1378
Glutamic acid, defects in metabolism of,
442f,
444f
Glutamic acid decarboxylase (GAD) deficiency,
447
Glutamic acid decarboxylase (GAD) transaminase deficiency,
447
Glutamic oxaloacetic transaminase in liver dysfunction evaluation,
1378
Glutamine
congenital deficiency of,
445
γ-Glutamylcysteine synthetase deficiency,
444
γ-Glutamyl transpeptidase (GGT)
Gluten, type 1 diabetes mellitus and early exposure to,
1972
Glycemic control in type 1 diabetes mellitus,
1984
D-Glyceric acid aciduria,
440
Glycerin suppositories,
74t
Glycerol for bacterial meningitis,
2094
Glycine
genetic disorders of,
445t
Glycogen storage diseases (GSDs),
492-501,
493f,
494t-495t,
748t,
751
cardiac manifestations of,
1531t
Fanconi-Bickel syndrome as,
499
glycogen synthetase deficiency as,
498
mimicking hypertrophic cardiomyopathy,
500
Glycoprotein syndrome, carbohydrate-deficient,
1311
Glycopyrrolate for respiratory secretions,
155t-156t
Glycosaminoglycan (GAG),
509,
514
Glycosylated hemoglobin (HbA
1A),
1984
Glycyrrhize glabra for asthma,
271t
Gonadotropin-independent precocious puberty, familial male,
1893
Gonadotropin-releasing hormone (GnRH)
for growth hormone deficiencies,
1881
in precocious puberty diagnosis,
1888
Gonadotropin-releasing hormone (GnRH) agonists
for precocious puberty,
1889
Gonadotropin-secreting tumors,
1891
Gonads
effects of eating disorders on,
92-93
ovaries as
pseudoprecocity resulting from lesions of,
1957-1958
testes as
pseudoprecocity resulting from tumors of,
1943-1950
Gonorrhea,
935-940
clinical manifestations of,
937
pathogenesis and pathology of,
936-937
prophylaxis following rape,
704,
704t
Goserelin acetate for precocious puberty,
1889
Graded exercise therapy for chronic fatigue syndrome,
e115-3
Graduated licensing law (GLL),
22
Graft coronary artery disease (GCAD),
e437-3
Graft failure, stem cell transplantation,
762
Graft thrombosis, renal transplantation,
e530-2
Graft
versus host disease (GVHD)
malabsorption due to,
1314
Gram-negative bacterial infections
due to
Haemophilus influenzae,
940-943
due to
Neisseria gonorrhoeae,
935-940
due to
Neisseria meningitidis,
929-935
due to
Pseudomonas aeruginosa,
975-977
Gram-positive bacterial infection
due to group A streptococcus,
914-925
due to group B streptococcus,
925-928
due to non-group A or B streptococci,
e178-1
due to
Streptococcus pneumoniae,
910-914
Granisetron for vomiting,
1244t
Granulocyte colony-stimulating factor (G-CSF)
Granulocyte macrophage-colony-stimulating factor (GM-CSF)
Granulocytopoiesis
primary disorders of,
750
Granuloma
caseating in nontuberculous mycobacteria,
1012
cholesterol, of tympanic membrane,
2212
Granulomatous disease
fever of unknown origin in,
900t
Granulomatous thyroiditis, subacute,
1905
Granulomatous vasculitis,
868t
Granulosa cell tumor, juvenile, ovarian,
1957-1958
Grasp response in neurologic examination,
e584-7
Gray platelet syndrome,
1722
Great arteries
malposition of with double-outlet right ventricle,
1588-1589
Great saphenous vein, venous access in,
292,
295f
Griscelli syndrome type II,
748t,
751
Gross motor development during first 2 years,
27t
Gross motor incoordination,
e29-2
Group A beta-hemolytic streptococci (GABHS)
glomerulonephritis development after,
1783-1785
in pharyngotonsillitis,
1443
Group A streptococcus (GAS),
914-925
differential diagnosis of,
918
obsessive-compulsive disorder associated with,
81
in toxic shock syndrome,
909
with varicella-zoster virus,
1109
Group B streptococcus (GBS),
925-928
laboratory findings in,
927
maternal
fetal and neonatal effects of,
e89-3t
Group therapy for eating disorders,
95
Growth and development
attachment and contingency and,
e6-2
behavioral during first year of life,
28t
caloric requirements for,
e13-3t
centers of ossification in,
29t
cognitive
during preschool years,
34
cystic fibrosis and,
1496
emotional
age 12-18 months,
31,
32t
during middle childhood,
38
during preschool years,
35-36
during first year,
26-31
developmental milestones in,
27t
linguistic
during preschool years,
34
during middle childhood,
36-39
moral
during middle childhood,
38
during preschool years,
35-36
physical
during middle childhood,
36-37
during preschool years,
33-34
of play during preschool years,
34-35
during preschool years,
33-36
psychologic influences on,
e6-2
during second year,
31-33
developmental milestones in,
27t
in skeletal dysplasias,
e685-1
social
during middle childhood,
38
theories of emotion and cognition in,
e6-3-e6-4
Growth factor
hematopoietic, for fever in neutropenic patient,
e171-1
recombinant for Fanconi anemia,
1686
vascular endothelial
in ovarian carcinomas,
1872t
in retinopathy of prematurity,
2174
in sudden infant death syndrome,
1422,
1427
Growth hormone (GH),
e550-1
deficiency and insensitivity of
abnormalities of growth hormone receptor in,
1879
clinical manifestations of,
1879
complications and adverse effects of,
1881
post-receptor forms of,
1879
radiologic findings in,
1880
for performance enhancement,
2423t
Growth hormone (GH) receptor,
e550-1
Growth hormone-releasing hormone (GHRH),
e550-1
Growth hormone-releasing hormone (GHRH) receptor, mutations in,
1878
Growth impairment
in congenital hypothyroidism,
1898
in failure to thrive,
147
in foreign-born adoptee,
131
after hematopoietic stem cell transplantation,
e133-1
due to immunosuppression therapy,
e437-3
due to inhaled corticosteroids,
793
in 3-methylglutaconic aciduria,
433
Growth-remaining charts, epiphysoidesis and,
e668-3f
Growth restriction, intrauterine,
555-564
definitions associated with,
555
gestational age at birth assessment in,
557,
558f
type 2 diabetes mellitus and,
1990
Grunting
during expiration in newborn,
535
as sign of respiratory pathology,
1420
Guanidinoacetate methyltransferase (GAMT) deficiency,
441
Guidance, anticipatory
health eating habits,
188t
in injury prevention,
19t
Gut, fetal development of,
1273
Gymnastics, injuries in,
2423t
Gynecological care for special needs girls,
1874-1875
Gyrate atrophy of retina and choroid,
453
H
Habit tic deformity,
2294
Haemophilus influenzae,
940-943
antibiotic resistance by,
941
in bacterial meningitis,
2087
clinical manifestations and treatment of,
941-943
Haemophilus influenzae type b
in septic arthritis,
2398
Haemophilus influenzae type b vaccine (Hib),
881t,
941t,
943
diphtheria acellular pertussis vaccine with (DTaP/Hib),
884t
with hepatitis B vaccine (Hib-HepB),
884t
recommended schedule for,
886,
887f
Hair
axillary, development of,
e555-1
effects of eating disorders on,
93t
effects of malnutrition on,
175t
over lumbosacral area in newborn,
533
pubic, sexual maturity ratings of changes in,
651f
repetitive pulling of,
75
structural defects of,
2292
Hair follicles, morphology of,
e636-1
Haller index on chest computed tomography,
1516
Hallopeau-Siemens epidermolysis bullosa,
2245t,
2246
Haloperidol,
63
for pain management,
364t
for psychosis and agitation,
64t
Haltia-Santavuori disease,
2073
Hamartoma
hypothalamus, precocious puberty due to,
1890
Hamartoma syndrome, overgrowth in,
e554-2t
Hand
arthrogryposis involving,
e674-5
Handwashing for prevention of neonatal infection,
647
Hantavirus in pneumonia,
1475t
Haplo-hematopoietic stem cell transplantation (HSCT),
e130-2
Haploinsufficiency,
e74-3
Hardy-Weinberg formula,
388
Harlequin color change,
2218
Hashimoto thyroiditis,
1903-1905
myasthenia gravis with,
2133
type 1 diabetes mellitus with,
1996
Head
centers of ossification appearance in,
29t
positioning of for bag-valve-mask ventilation,
284-285,
285f
Head and neck block for pain management,
371
Head circumference
in neurologic examination,
e584-2
Head computed tomography (CT)
HEADSS screening interview,
57,
57t
Healing of fracture,
2389
Health
among postinfancy children,
2-4
Health care
for at-risk populations,
10-11
Health care providers
infection control and prevention for,
e166-4
obesity prevention and,
187t
training of for emergencies,
e61-1
Health care reform, effects on quality,
e2-7
Health information technology (HIT),
e2-7
Health Insurance Portability and Accountability Act of 1996 (HIPAA)
on adolescent confidentiality,
e106-2
Health InterNetwork Access to Research Initiative (HINARI),
e61-16
Health risk behaviors in adolescents,
661f
Hearing impairment or loss,
2188-2196
in cleft lip and palate,
1253
due to congenital rubella syndrome,
1077-1078
familial, cardiac manifestations of,
1531t
genetic counseling in,
2196
incidence and prevalence of,
2188
language disorders due to,
119
due to toxoplasmosis,
1213
in X-linked adrenoleukodystrophy,
468
Heart disease
failure to thrive in,
148t
phosphorylase kinase deficiency as,
498
psychopharmacology and,
65
renal transplantation and,
e530-2
Heart murmur
infective endocarditis and,
1623
Heart rate
fetal
in biophysical profile,
543t
neonatal resuscitation and,
575-576
Heart sounds
in acutely ill child evaluation,
276
in cardiac examination,
1533
Heart tube, embryonic,
1527
Height
See also Length
for age, in nutrition assessment,
172
Heliotrope rash of juvenile dermatomyositis,
846-847
Helmet for bicycle injury prevention,
22-23
Helminthic disease
Gnathostoma spinigerum,
1227
Helper T cells
development and differentiation of,
e117-1
in Epstein-Barr virus,
1111
interaction with other immune cells,
e117-5
Hemagglutinin protein in influenza virus,
1122
Hemangioendothelioma,
1762t
Hemangiopericytoma,
1762t
Hematocrit
in abnormal uterine bleeding,
688-690
Hematoma
subdural, due to child abuse,
139,
139f
Hematopoietic growth factor for fever in neutropenic patient,
e171-1
Hematopoietic stem cell transplantation (HSCT),
757
for acute lymphocytic leukemia,
757,
758f
for acute myeloid leukemia,
757-758
for Chédiak-Higashi syndrome,
744-745
for chronic myelogenous leukemia,
758
for Diamond-Blackfan anemia,
1651
fungal infection associated with,
1055
for immunodeficiency disorders,
760
for juvenile myelomonocytic leukemia,
758
for Lesch-Nyhan disease,
e83-5
for leukocyte adhesion deficiency,
744
for mucopolysaccharidoses,
514
for myelodysplastic syndromes,
758-759
for non-Hodgkin lymphoma,
759
pancytopenia caused by,
1692
for X-linked adrenoleukodystrophy,
468-469
Hematopoietic syndrome, duet to whole-body irradiation,
e699-4
Hematuria
anatomic abnormalities associated with,
1796-1799
due to autosomal dominant polycystic kidney disease,
1798,
1798f
in glomerulonephritis associated with systemic lupus erythematosus,
1788-1789
in Henoch-Schönlein purpura nephritis,
1789
due to idiopathic hypercalciuria,
1795
isolated glomerular disease with recurrent gross,
1781-1783
lower urinary tract causes of,
1799
in membranoproliferative glomerulonephritis,
1787-1788
in thin basement membrane disease,
1783
due to vascular abnormalities,
1794
due to vigorous exercise,
1799
Hemiconvulsion, hemiplegia, epilepsy (HHE) syndrome,
2038
Hemifacial microsomia,
1254
Hemin for acute intermittent porphyrias,
e85-7
Hemiplegic migraine,
2042
Hemochromatosis
cardiac manifestations of,
1531t
Hemodialysis
for end-stage renal disease,
1826
for metabolic acidosis,
235
for poisoning with toxic alcohols,
268
Hemodynamics of ventricular septal defect,
1557-1558
Hemoglobin A
1C in obesity,
185t
Hemoglobin (Hb)
in abnormal uterine bleeding,
688-690
in congenital dyserythropoietic anemia,
e446-1t
in hereditary spherocytosis,
1660
in systemic-onset juvenile idiopathic arthritis,
836
Hemoglobinopathies,
1662-1677
abnormal hemoglobins causing cyanosis as,
1672
abnormal hemoglobins with increased oxygen affinity as,
1671
syndromes of hereditary persistence of fetal hemoglobin as,
1673-1674
Hemoglobin S (Hb S),
1663
Hemolysis
in congenital erythropoietic porphyria,
e85-9
Hemolytic anemia
due to bartonellosis,
982
enteric infection and,
1333t
after Epstein-Barr virus infection,
1114
due to extracellular factors,
e459-1
hemoglobinopathies as,
1662-1677
abnormal hemoglobins causing cyanosis as,
1672
abnormal hemoglobins with increased oxygen affinity as,
1671
syndromes of hereditary persistence of fetal hemoglobin as,
1673-1674
hereditary elliptocytosis as,
e453-1
hereditary stomatocytosis as,
e454-1
parvovirus B19 infection and,
1095
Hemolytic disease of newborn,
615-619,
620t
due to ABO incompatibility,
619
Hemoptysis
as manifestation of extrapulmonary disease,
e413-1t
Hemorrhage/bleeding
into adrenal glands,
1927
as delivery room emergency,
578
cardiac arrest due to,
289t
in chronic kidney disease,
1823t
endobronchial, in cystic fibrosis,
1493
perifollicular, due to vitamin C deficiency,
198-199,
199f
retinal
neurologic examination of,
e584-3
subarachnoid
emergency management of,
304
transplacental, anemia due to,
612-613
vitamin K-deficiency,
210
Hemorrhagic conjunctivitis, due to enterovirus,
1091
Hemorrhagic corpus luteum,
1871
Hemorrhagic cystitis,
1799
Hemorrhagic cystitis, acute,
1830
Hemorrhagic disorders
acquired inhibitors of coagulation in,
1712-1713
clinical and laboratory evaluation of,
1696-1699
hereditary clotting factor deficiencies as,
1699-1704
due to liver disease,
1712
platelet and blood vessel disorders as,
1714
postnatal vitamin K deficiency as,
1712
Hemorrhagic edema, acute,
870
Hemorrhagic fever with renal syndrome (HFRS),
1151-1154
Hemorrhagic measles,
1072
Hemorrhagic telangiectasia, hereditary,
2230
Hemosiderinuria in congenital dyserythropoietic anemia,
e446-1t
Henderson-Hasselbach equation,
e52-13
Henoch-Schönlein purpura (HSP),
868-871,
868t,
869f-870f,
870t,
874t,
1722,
e147-1
alveolar hemorrhage with,
1499
nephritis associated with,
1789
scrotal involvement in,
1863
Heparin
low molecular weight,
1711
possible adverse reactions to in premature infant,
563t
for pulmonary embolism,
1502
Hepatic arteriovenous fistula,
e438-1
Hepatic crisis in tyrosinemia,
422
Hepatic encephalopathy,
1414t
Hepatic lipase deficiency,
473t,
477
Hepatic tumor, precocious puberty due to,
1891
Hepatitis
congenital alloimmune,
1393
psychopharmacology and,
64-65
Hepatitis A vaccine (HepA),
884t,
1396
with hepatitis B vaccine (HepA-HepB),
884t
Hepatitis B arthirtis-dermatitis syndrome,
840
Hepatitis B e antigen (HBeAg),
1397
Hepatitis B s antigen (HBsAg),
1397
Hepatitis B vaccine (HepB),
884t,
1399-1400,
1399t
with diphtheria acellular pertussis vaccine and inactivated polio vaccine (DTaP-HepB-IPV),
884t
with
Haemophilus influenzae type b vaccine (Hib-HepB),
884t
with hepatitis A vaccine (HepA-HepB),
884t
Hepatitis C,
1400-1402,
1400f
hypothyroidism due to,
1901
in immigrant children,
133
maternal
fetal and neonatal effects of,
e89-3t
in porphyria cutanea tarda,
e85-11
Hepatobiliary tract disorders
due to typhoid fever,
957t
Hepatocellular carcinoma,
1772
in type II glycogen storage disease,
496
Hepatoportoenterostomy procedure,
1387
Hepatopulmonary syndrome,
1376
Hepatorenal syndrome (HRS),
1376
Hepatosplenomegaly, due to cat-scratch disease,
985,
985f
Herbal medicine,
270-273,
271t-272t
for atopic dermatitis,
805
nutritional aspects of,
169
Spanish-English translation chart,
274t
Hereditary clotting factor deficiencies,
1699-1704
Hereditary hemorrhagic telangiectasia (HHT),
2230
Hereditary hypophosphatemic rickets with hypercalciuria (HHRH),
207
Hereditary motor-sensory neuropathies (HMSNs),
2138-2140
Hereditary nonpolyposis colon cancer (HNPCC),
1773
Hereditary osteoarthro-ophthalmopathy,
2426,
2426f
Hereditary periodic fever syndromes,
855-860,
855t-856t
chronic infantile neurologic cutaneous and articular disease as,
858
familial cold autoinflammatory syndrome as,
858
hyperimmunoglobulinemia D syndrome as,
857-858
Muckle-Wells syndrome as,
858
periodic fever, aphthous stomatitis, pharyngitis, and adenitis as,
859-860
pyogenic arthritis, pyoderma gangrenosum, and acne syndrome as,
858-859
tumor necrosis factor receptor-associated periodic syndrome as,
858,
859f
Hereditary stomatocytosis,
e454-1
Hereditary xanthinuria,
e83-7
Hering-Breuer inflation index,
1421
Herlyn-Werner-Wunderlich syndrome (HWWS),
e548-2
Hernia/herniation
intervertebral disk,
2377
Herpes gestationis, immunofluorescence of,
e637-1t
Herpes simplex virus (HSV),
1097-1104
atopic dermatitis and,
806
exclusion from day care due to,
e15-2t
in immunocompromised patients,
1101
immunofluorescent-antibody testing of,
e164-3
laboratory findings in,
1102
maternal
fetal and neonatal effects of,
e89-3t
predisposition to infection due to immunodeficiency,
716t
in viral meningoencephalitis,
2096
Herring lateral pillar classification,
2362,
2362f
Heterophile antibody test for Epstein-Barr virus,
1113
Heterotopic heart transplantation,
e437-1
Heterozygotes
detection in cystic fibrosis,
1490
Heterozygous, defined,
e56-1
Heterozygous familial hypercholesterolemia (FH),
474
Hexachlorophene, possible adverse reactions to in premature infant,
563t
Hexane, as inhalant,
681t
Hexose monophosphate pathway, deficiencies of enzymes of,
1678
Hibernian fever, familial,
858
Hickman catheter infection,
e172-1
Hidradenitis suppurativa,
2288
Hidrotic ectodermal dysplasia,
2223
High-altitude pulmonary edema (HAPE),
1469
High-density lipoproteins (HDL),
471,
472f,
472t,
479t
disorders of metabolism of,
477
reverse cholesterol transport and,
473
High-efficiency particulate air (HEPA) filter,
769
High-frequency jet ventilation (HFjV),
326-327
High-frequency oscillation (HFO),
326
High-frequency ventilation (HFV),
326-327
High-grade squamous intraepithelial lesion (HSIL),
1138t
Highly active antiretroviral therapy (HAART),
1159
High molecular weight kininogen (HMWK)
reference values for,
1698t
High-quality child care,
e15-3
High-tension electrical wire burn,
356
Hip
arthrogryposis involving,
e674-4
centers of ossification appearance in,
29t
dislocation of, with arthrogryposis,
e674-4
disorders of,
2355-2365
slipped capital femoral epiphysis as,
2363,
2364f
transient monoarticular synovitis as,
2360
growth and development of,
2355
musculoskeletal pain syndrome of,
877t
normal development of,
2344
Hirschberg corneal reflex,
2157
Hispanic population
disease beliefs or practices of,
e4-2t
Histamine
genetic disorders of,
445t
in neuroendocrine tumor-associated diarrhea,
e333-2t
Histamine-2 receptor antagonists (H2RAs)
for gastroesophageal reflux disease,
1268
for peptic ulcer disease,
1294
Histamine
1-type antihistamines,
771,
771t
Histerlin for precocious puberty,
1889
Histidine, defects in metabolism of,
453
Histidine decarboxylase deficiency,
447
Histone antibody in rheumatic disease,
e147-3t
History
in attention deficit/hyperactivity disorder,
109-110
in fever of unknown origin,
899-901
in gynecological problems,
1865
in intellectual disability,
127t
in respiratory disease,
e366-1
History of pediatrics,
1-5
HIV/AIDS,
1157-1177
adrenal insufficiency with,
1925t
bacillary angiomatosis in,
986
cardiovascular system involvement,
1165
central nervous system involvement in,
1164-1165
fever without a focus in,
896t
gastrointestinal and hepatobiliary tract involvement in,
1165
hematologic and malignant disease due to,
1166
in immigrant children,
134
inflammatory bowel disease
versus enteropathy of,
1298t
maternal
fetal and neonatal effects of,
e89-3t
in porphyria cutanea tarda,
e85-11
prophylaxis following rape,
704,
704t
respiratory tract involvement in,
1165
skin manifestations of,
1166
as threat to homosexual youth,
659
Hoarseness, due to gastroesophageal reflux disease,
1269
Hodgkin disease
Epstein-Barr virus-associated,
1112
hematopoietic stem cell transplantation for,
759
Holocarboxylase synthetase (HCS) deficiency,
432
secondary to pyruvate carboxylase deficiency,
506
Holosystolic murmur,
1535
Holter recordings in supraventricular tachycardia,
1614-1615
Home care
of asthma exacerbations,
799
of child with life-threatening illness,
151
of premature or low birthweight infant,
564
Home monitoring
in congenital central hypoventilation syndrome,
1522
for sudden infant death syndrome prevention,
1428-1429
Homeostatic process in sleep,
46
Homocysteine testing,
1699
Homozygous, defined,
e56-1
Homozygous hypobetalipoproteinemia,
1313
Homozygous variegate porphyria,
e85-1t
Honeybee, allergic responses to,
807f
Horizontal transmission,
385
Hornet, allergic responses to,
807f
Hospital
emergency care in, in developing world,
e61-15
international resources associated with care in,
e61-14t
referring, responsibility of in transport medicine,
e61-8-e61-9
Hospitalization
for eating disorders,
95t
for Kawasaki disease,
863
in patterns of health care,
9
Host factors
in
Neisseria meningitidis infection,
931
Household products, poisoning with,
266-268
HSD3B7 gene defect,
1383t
Human African trypanosomiasis (HAT),
1190-1193
Human chorionic gonadotropin
in ovarian carcinomas,
1872t
Human coronavirus 229E (HCoV-229E),
1134
Human coronavirus HKU1 (HCoV-HKU1),
1134
Human coronavirus NL63 (HCoV-NL63),
1134
Human coronavirus OC43 (HCoV-OC43),
1134
Human factors engineering (HFE),
e2-6
Human genome,
e74-1-e74-5
genotype-phenotype correlations in genetic disease and,
e74-4
Human herpesviruses 8 (HHV-8),
1121
malignancy susceptibility associated with,
e486-3
Human immunodeficiency virus
See HIV/AIDS
Humanitarian efforts for protection of children from effects of war,
e36-6-e36-7
Human leukocyte antigen (HLA)-B27
in reactive arthritis,
839
Human leukocyte antigen (HLA)-B51,
854
Human leukocyte antigen (HLA)-DQA1*05,
1308
Human leukocyte antigen (HLA)-DQA1*0501,
846
Human leukocyte antigen (HLA)-DQB1*02,
1308
Human leukocyte antigen (HLA)-DRB*0301,
846,
1308
Human leukocyte antigen (HLA)-DRB*0302,
1308
Human leukocyte antigen (HLA) matching for stem cell transplantation,
757
Human papillomavirus (HPV),
1137-1141
differential diagnosis of,
1140
predisposition to infection due to immunodeficiency,
716t
prophylaxis following rape,
704t
Human recombinant DNase,
1491
Humerus, centers of ossification appearance in,
29t
Humidifier hypersensitivity pneumonia,
1473
Humidity, thermoregulation in premature infant and,
559
Humoral immunodeficiencies, infection with,
e171-3
Humulus lupulus for sedation,
271t
Hutchinson syndrome,
1754t
Hyaluronidase deficiency,
512t
Hydoxocalamin as poisoning antidote,
256t-257t
Hydralazine
for hypertensive emergencies,
1646t
for systemic hypertension,
1645t
Hydration
cutaneous, for atopic dermatitis,
804
withholding of artificial,
e3-2
Hydrochlorothiazide for systemic hypertension,
1645t
Hydrocodone for pain management,
365t
Hydrogen cyanide poisoning,
270
Hydromorphone
equianalgesic doses and half-life of,
367t
for pain management,
365t
Hydrops fetalis
nonimmune, in congenital erythropoietic porphyria,
e85-9-e85-10
parvovirus B19 infection and,
1095,
1653
Hydroxocobalamin for cyanide poisoning,
270,
e704-8
3-Hydroxyacyl CoA dehydrogenase deficiency
β-Hydroxy-β-methylglutaryl CoA (HMG CoA) synthase deficiency,
461-462
γ-Hydroxybutyrate, adolescent abuse of,
675t
γ-Hydroxybutyric aciduria,
447
Hydroxychloroquine
for juvenile dermatomyositis,
849
for lupus erythematosus profundus,
2283
for porphyria cutanea tarda,
e85-12
for systemic lupus erythematosus,
844
3β-Hydroxy C
27-steroid dehydrogenase (3β-HSD) deficiency,
1384
Hydroxymethylbilane (HMB),
e85-2f
3-Hydroxy-3-methylglutaric aciduria,
435
3-Hydroxy-3-methylglutaryl (HMG) CoA synthase deficiency, mitochondrial,
435
4-Hydroxyphenylpyruvate dioxygenase deficiency,
423
Hydroxyproline malabsorption,
1319
3β-Hydroxysteroid dehydrogenase (3β-HSD) deficiency,
1932t,
1936
3β-Hydroxysteroid dehydrogenase deficiency,
1925t,
1964
17β-Hydroxysteroid dehydrogenase deficiency,
1959-1961
Hydroxyurea for sickle cell disease pain,
1665
Hydroxyzine
for depression and anxiety symptoms,
63t
Hygiene
for gastroenteritis prevention,
1338
for herpes simplex virus prevention,
1103
oral, for dental caries prevention,
1256
Hyoscyamine sulfate for respiratory secretions,
155t-156t
Hyperacusis in Tay-Sachs disease,
485
Hyperacute rejection of renal transplantation,
e530-5
hyperammonemia-hyperornithinemia-homocitrullinemia (HHH) syndrome,
453
Hyperbaric oxygen (HBO) for carbon monoxide poisoning,
270
Hyperbilirubinemia
inherited conjugated,
1390
nomogram for risk assessment of,
e708-11f
pyloric stenosis with,
1274
unconjugated
differential diagnosis of,
1376t
Hypercalcemia
etiologic classification of,
1921t
due to hyperparathyroidism,
1921
with subcutaneous fat necrosis,
2284
Hypercalciuria
hereditary hypophosphatemic rickets with,
207
Hypercapnia, due to surfactant deficiency,
582
Hypercapnia, permissive,
585
Hypercarbia, chronic, respiration regulation in,
e365-17
Hypercholanemia, familial,
1384
Hypercoagulable states, renal transplantation and,
e530-2
Hypercyanotic attacks in tetralogy of Fallot,
1574
“Hyperdynamic pulmonary hypertension”,
1557
Hypereosinophilic syndrome,
740
Hyperfiltration injury in chronic kidney disease,
1822
Hypergammaglobulinema in HIV infection,
1161
Hyperglobulinemia in kala-azar,
1189
Hyperglycemia
plasma osmolality and,
e52-2
Hypergonadotropic hypogonadism
Hyperimmune animal antisera preparations,
882-883
Hyperimmune globulin preparations,
882
Hyperimmunoglobulinemia D syndrome (HIDS),
855t,
857-858
Hyperinfection syndrome of strongyloidiasis,
1223
Hyperinsulinemic state,
518
Hyperkalemia,
219-222
in acute renal failure,
1820
cardiac arrest due to,
289t
in chronic kidney disease,
1823t
clinical manifestations of,
221
electrocardiogram of,
1541f
Hyperkalemic renal tubular acidosis,
1810-1811
Hyperleukocytosis as oncologic emergency,
e488-6t
Hyperlipidemia
in chronic kidney disease,
1823t
secondary causes of,
477t
Hyperlipoproteinemias,
473-482,
473t
blood cholesterol screening for,
479-480
conditions associated with low cholesterol as,
477-478,
478t
high-density lipoproteins metabolism disorders as,
477
intracellular cholesterol metabolism disorders as,
478-479
Hyperlucent lung, unilateral,
1461
Hypermobile Ehlers-Danlos syndrome,
2278
Hypermobile pes planus (flatfoot),
2338,
2338f
Hypermobility syndrome, benign,
e147-1
Hypermyelinating neuropathy,
2140
Hyperparathyroidism-jaw tumor syndrome,
1921
Hyperplasia
β-cell in hyperinsulinemia,
521-522
congenital adrenal,
1930-1939,
1931f
adrenocortical insufficiency due to,
1924
due to 3β-hydroxysteroid dehydrogenase deficiency,
1936
metabolic alkalosis in,
236
Hyperprolactinemia
delayed puberty due to,
1949
Hypersensitivity
in adverse drug reactions,
824
cutaneous manifestations of,
e637-3t
fever of unknown origin in,
900t
in tuberculosis pathogenesis,
998
Hypersensitivity angitis,
868t
Hypersensitivity vasculitis,
876,
876t
Hypertension
in acute renal failure,
1821
due to immunosuppression therapy,
e437-3
with type 2 diabetes mellitus,
1993t
Hypertensive encephalopathy,
2068
strokelike events
versus,
2086
Hyperthyroxinemia, familial dysalbuminemic,
e558-1
Hypertonic saline for cystic fibrosis,
1491
Hypertriglycerides, hypercholesterolemia with,
475-476
Hypertrophic gastropathy,
1276
Hypertrophic osteoarthropathy,
e163-1
Hypertrophy
assessment in neurologic examination,
e584-6
ventricular
radiographic assessment of,
1537
systemic hypertension with,
1642
Hyperuricemia as oncologic emergency,
e488-6t
Hyperventilation
for persistent pulmonary hypertension of the newborn,
593
respiratory alkalosis and,
241
Hyperventilation spell, seizure
versus,
e587-4
Hyperviscosity in plethora,
619
Hypervolemic hyponatremia,
216,
218
Hypnosis as goal of anesthesia,
e70-1
Hypnotherapy for pain management,
371
Hypoalbuminemia in protein losing enteropathy,
1307
Hypoalphalipoproteinemia,
477
Hypocalcemia
in acute renal failure,
1821
etiologic classification of,
1917t
Hypocellular marrow,
1684
Hypochloremic alkalosis in cystic fibrosis,
1487
Hypochromic microcytic anemia,
e450-1
Hypocomplementemic urticarial vasculitis,
876
Hypodysplasia, renal,
1827
Hypoglycemia,
517-531
with adrenal insufficiency,
1927
diagnosis and differential diagnosis of,
524t,
530
in infants of diabetic mothers,
628
management of in protein-energy malnutrition,
178t
neonatal seizures due to,
2034
significance and sequelae of,
517-518
stroke-like events
versus,
2085
in type 1 diabetes mellitus,
1985
in type I glycogen storage disease,
492-493
Hypogonadism
hypergonadotropic, gynecomastia with,
1950-1951
Hypogonadotropic hypogonadism (HH)
Hypokalemia,
222-224
cardiac arrest due to,
289t
clinical manifestations of,
224
electrocardiogram of,
1540f
with primary aldosteronism,
e572-1
Hypolactasia, primary adult type,
1317
Hyponatremia
in acute intermittent porphyrias,
e85-6
in acute renal failure,
1821
in diabetes insipidus,
215-219
clinical manifestations of,
217
differential diagnosis of,
1884t
emergency treatment of,
1886
hypothyroidism-associated,
1903t
neonatal seizures due to,
2034
Hypophosphatemic rickets,
202t
autosomal recessive,
202t
due to Fanconi syndrome,
207
hereditary with hypercalciuria,
207
Hypopigmentation
genes associated with,
2238t
Hypopituitarism,
1876-1881
abnormalities of growth hormone receptor in,
1879
clinical manifestations of,
1879
hypogonadotropic hypogonadism with,
1956
psychosocial causes of,
1881
radiologic findings in,
1880
treatment of,
1881
complications and adverse effects of,
1881
Hypoplasia
lymphoid in X-linked agammaglobulinemia,
724
of mandible, as delivery room emergency,
575
pulmonary,
1464
with congenital diaphragmatic hernia,
594
due to oligohydramnios,
e89-2
Hypotension
during induction of anesthesia,
e70-8
Hypothalamus
See also Pituitary gland disorders
fever of unknown origin due to dysfunction of,
901
hamartoma of, precocious puberty with,
1890
hypothyroidism due to disease of,
1901
puberty physiology and,
e555-1
Hypothermia
cardiac arrest due to,
289t
hypothyroidism-associated,
1903t
induced
for hypoxic-ischemic encephalopathy,
302,
571
in post-resuscitation care,
296
management of in protein-energy malnutrition,
178t
Hypothyroidism,
1895-1903
cardiac manifestations of,
1531t
due to iodine deficiency,
e51-1
precocious puberty and,
1891
due to total body irradiation,
e133-1
Hypothyroxinemia of prematurity,
627
Hypotonia
assessment in neurologic examination,
e584-6
Hypoventilation, alveolar,
1523
Hypovolemia
cardiac arrest due to,
289t
with fulminant hepatic failure,
1414
Hypovolemic shock,
285,
307t
clinical manifestations of,
308
hemodynamic variables in,
311t
Hypoxanthine-guanine phosphoribosyltransferase (HPRT) deficiency,
e83-3-e83-5
Hypoxemia,
1419
permissive, in mechanical ventilation for respiratory distress syndrome,
585
Hypoxia
cardiac arrest due to,
289t
chronic, respiration regulation in,
e365-17
due to surfactant deficiency,
582
tissue, respiratory alkalosis due to,
240,
241t
Hypoxic-ischemic insult, global,
301-303
I
Iatrogenic cryptorchidism,
1367
Ibuprofen
for juvenile idiopathic arthritis,
838t
for pain management,
364t
Ice hockey, injuries in,
e684-2
I-cell disease mucolipidosis type II,
1523
Ichthyosiform erythroderma,
2268t
Icteric leptospirosis,
1024
Icteropyloric syndrome,
1274
Idarubicin for cancer therapy,
e488-4t
Identity
adolescent formation of,
650t
Idiopathic pulmonary hemorrhage (IPH),
1498-1500
IEP
See Individualized education program (IEP)
Ifosfamide for cancer therapy,
e488-4t
IL-1β
See Interleukin-1β (IL-1β)
Ileoileal intussusception,
1289
Iliohypogastric nerve block,
372
Ilioinguinal nerve block,
372
Illicium anisatum, potential toxicity of,
272t-273t
Illness
integrated management of childhood and,
1334,
1335f
Iloprost for pulmonary hypertension,
1602t
Imaging studies
See also Radiology
in acute disseminated encephalomyelitis,
2079
in chronic diarrhea,
1344
in febrile seizures,
2018
in intellectual disability,
127t
in malabsorption disorders,
1308
in neuromuscular disorders,
2111
in orthopedic problems,
2334
Imerslund-Grasbeck syndrome,
1320
Imipenem-cilastin for cystic fibrosis lung infection,
1492t
Imipramine
for attention deficit/hyperactivity disorder,
111t
for depression and anxiety symptoms,
63t
for nocturnal incontinence,
1852
Imiquimod
for human papillomavirus,
1140
Immersion burn, due to child abuse,
138
Immigrant children,
6-7
effects of relocation on,
e16-2
Immobility
hypercalcemia due to prolonged,
1923
Immune complexes
in adverse drug reactions,
824
Immune dysregulation, polyendocrinopathy, enteropathy, X-linked (IPEX) syndrome,
738,
1312,
1341,
1969,
1995
Immune reconstitution inflammatory syndrome (IRIS),
1162
Immunity
to group B streptococci,
926
to Haemophilus influenzae,
941,
941t
Immunization(s),
881-895,
881t See also Vaccine(s)
chronic kidney disease and,
1825
congenital heart disease and,
1603
for homosexual youth,
659
immigrant children and,
132,
134
international practices on,
893-895
maternal, group B streptococcus,
928
National Immunization Days and,
1087
precautions and contraindications for,
892-893
sudden infant death syndrome and,
1425
type 1 diabetes mellitus and,
1972
websites and resources associated with,
894t
Immunocompromised patient
bacillary angiomatosis in,
986
fever without a focus in,
896t
infections in,
e171-1-e171-9,
e171-1t
with B cell defects (humoral immunodeficiencies),
e171-3
with defective splenic function, opsonization, and complement activity,
e171-2-e171-3
with phagocytic defects,
e171-2
with primary immunodeficiencies,
e171-2
Pseudomonas aeruginosa,
976
with T cell defects (cell-mediated immunodeficiencies),
e171-3
varicella-zoster virus,
1107
Immunodeficiency(ies),
715-722,
716t,
721t
antibody,
722-728,
724f
hyper-immunoglobulin M syndrome as,
726-727
immunoglobulin A deficiency as,
725
immunoglobulin G subclass deficiencies as,
725-726
immunoglobulin heavy- and light-chain deletions as,
726
X-linked lymphoproliferative disease as,
727
cellular,
728-729,
728t
autoimmune polyendocrinopathy-candidiasis ectodermal dysplasia as,
730
CD8 lymphocytopenia as,
730
defective cytokine production as,
729
defective expression of T-cell receptor-CD3 complex as,
729,
729f
hematopoietic stem cell transplantation for,
760
inheritance in development of,
e117-6
prenatal diagnosis and carrier detection in,
e117-6
pulmonary manifestations of,
e413-1t
red blood cell aplasia in,
1653
with thrombocytopenia and eczema,
734-735
Immunofluorescence studies
in parainfluenza viruses,
1125t
Immunofluorescent-antibody (IFA) technique,
e164-3
Immunoglobulin(s),
882t
administered with measles vaccine,
1074,
1074t
heavy- and light-chain deletions of,
726
intravenous,
882t
for cytomegalovirus prophylaxis,
1117
for idiopathic thrombocytopenic purpura,
1717
for myasthenia gravis,
2135
specific preparations of,
882,
882t
for urticaria and angioedema,
815t
in neonatal immunity,
631
subcutaneous, for B-cell defects,
727-728
Immunoglobulin A (IgA)
in Henoch-Schönlein purpura,
868-869
in screening for B cell defects,
719
Immunoglobulin A (IgA) dermatosis, linear,
2249,
2249f
Immunoglobulin E (IgE)
in adverse drug reactions,
824
anti-
for allergic disease,
772
for atopic dermatitis,
805
in atopic dermatitis,
802
in nonallergic disease,
767t
in urticaria and angioedema,
811
Immunoglobulin G (IgG),
e164-4
in adverse drug reactions,
824
deficiencies of
in common variable immunodeficiency,
725
in neonatal immunity,
631
in screening for B cell deficiencies,
720
Immunoglobulin G indirect fluorescent-antibody (IgG-IFA) testing, in toxoplasmosis,
1213
Immunoglobulin M enzyme-linked immunosorbent assay (IgM-ELISA), in toxoplasmosis,
1213-1214
Immunoglobulin M (IgM)
in adverse drug reactions,
824
in arboviral encephalitis,
1144
Immunoglobulin M indirect fluorescent-antibody (IgM-IFA) testing, in toxoplasmosis,
1213
Immunoproliferative small intestinal disease (IPSID),
1314-1315
Immunosorbent agglutination test (ISAGA), in toxoplasmosis,
1214
Immunosuppression
cutaneous manifestations in setting of,
e637-6
dental problems associated with,
1251t
for intestinal transplantation,
e331-2
for liver transplantation,
e360-1
Immunosuppression, pharmacokinetics and,
e56-3t
Implant
progestin, for special needs girls,
1875
Impramine for nocturnal enuresis,
73t
Impulsivity, psychopharmacologic management of,
61t
Inactivated polio vaccine (IPV),
884t,
1087-1088
with diphtheria acellular pertussis vaccine and hepatitis B vaccine (DTaP-HepB-IPV),
884t
with diphtheria acellular pertussis vaccine (DTaP-IPV),
884t
with diphtheria acellular pertussis vaccine
Haemophilus influenzae type b vaccine (DTaP-IPV/Hib),
884t
Inattention, psychopharmacologic management of,
61t
Inborn errors of metabolism,
416-418
of amino acids,
418-456
malabsorption due to,
1318
of valine, leucine, isoleucine, and related organic acidemias,
430-438,
430f
cardiac manifestations of,
1531t
common characteristics of,
416
metabolic acidosis due to,
233
myocardial disease with,
1629t
neonatal seizures due to,
2036
physiologic therapies for,
379
severe intellectual disability in,
123t
strokelike events
versus,
2086
Incarcerated inguinal hernia,
1365
Increased intracranial pressure (ICP),
297
migraine secondary to,
2046
Indeterminate leprosy (IL),
e208-1
Indian childhood cirrhosis,
1392
Indian Health Service,
10
Indirect cystography,
1836
Indirect fluorescent-antibody testing, in toxoplasmosis,
1213
in intellectual disability,
128
Individualized family service plan (IFSP),
e15-4
in intellectual disability,
128
Individuals with Disabilities Education Act (IDEA),
122-123,
e15-4
Indomethacin
possible adverse reactions to in premature infant,
563t
for prevention of intraventricular hemorrhage,
568
Induction of general anesthesia,
e70-5-e70-8
adverse reactions to agents used for,
827
parenteral presence during,
e70-8
Infant
See also Newborn
behavioral and psychosocial assessment of,
56
child restraint in motor vehicles for,
21t
disruptive behavioral disturbances in,
99
drowning or submersion injury to,
342
fever without a focus in,
896t
gonococcal infection in,
939
gynecological examination of,
e542-1
intellectual disability in,
125t
leading causes of death for,
5t
perception and effects of pain on,
373-375
Infantile acropustulosis,
2220
Infantile encephalopathy, early epileptic,
2023
Infantile parkinsonism,
445
Infantile polyarteritis nodosa,
862-867
Infantile Refsum disease,
464,
466t
Infarction
periventricular hemorrhage,
566
Infection(s)
adrenocortical insufficiency due to,
1927
anaerobic
Clostridium difficile infection as,
994-995
atopic dermatitis and,
806
central nervous system,
2086-2098
neonatal seizures due to,
2034
Staphylococcus aureus,
905
stroke-like events
versus,
2085
failure to thrive in,
148t
hematopoietic stem cell transplantation-related,
762-763
in immunocompromised patient,
e171-1-e171-9,
e171-1t
with B cell defects (humoral immunodeficiencies),
e171-3
with defective splenic function, opsonization, and complement activity,
e171-2-e171-3
with phagocytic defects,
e171-2
with primary immunodeficiencies,
e171-2
Pseudomonas aeruginosa,
976
international health care and,
e61-12
international prevention of,
e61-12
juvenile idiopathic arthritis and,
835
mycobacterial
predisposition to due to immunodeficiency,
716t
neonatal,
629-648
complications and prognosis for,
646,
647t
Haemophilus influenzae in,
943
systemic inflammatory response syndrome due to,
637-639
varicella-zoster virus,
1106
with nephrotic syndrome,
1805
perinatal
congenital lymphocytic choriomeningitis,
548
prevention of
in premature and low birthweight infants,
353-354
as protection against diabetes mellitus,
1972
renal transplantation and,
e530-2
respiratory tract
group A streptococcus in,
916
Staphylococcus aureus in,
905
serologic diagnosis of,
e164-4
systemic inflammatory response syndrome and,
309t
urinary tract,
1829-1834
coagulase-negative staphylococci in,
910
prevalence and history of,
1829
wound
following inguinal surgery repair,
1367
Infection-associated hemophagocytic syndrome (IAHS),
1774,
1774t
Infection prevention and control committee,
e166-1
Infection preventionists,
e166-1
Infectious mononucleosis-like illness,
1110
Infective endocarditis,
1622-1626
acute rheumatic fever
versus,
923,
923t
congenital heart disease and,
1609
dental procedures prophylaxis,
1626t
prognosis and complications of,
1624
in tetralogy of Fallot,
1576
Infertility
inguinal hernia repair and,
1368
Infestation
seabather’s eruption,
2322
Infiltrates, lung
in acute lung injury,
317f
Infiltration, bone marrow,
1684
Inflammation
cutaneous, pigmentary changes due to,
2238
cytokines in regulation of,
e117-3t
Inflammatory diarrhea,
1330
Inflammatory mediators in neonatal immunity,
632
Infliximab
for juvenile idiopathic arthritis,
838t
Information explosion of 21st century,
11-12
Information technology, quality improvement and,
e2-7
Infundibular stenosis,
1841
pulmonary valve,
1564
ventricular septal defect with,
1558
Inguinal undescended testis,
1859
Inhaled β-agonists for asthma
Inhaled corticosteroids (ICs)
Inhaled gases for respiratory distress and failure,
319-320
Inhaled nitric oxide (iNO)
for congenital diaphragmatic hernia,
595
for persistent pulmonary hypertension of the newborn,
593
for respiratory distress and failure,
319,
586
Inherent strengths in special risk populations,
8-9
Inheritance
in immunodeficiency development,
e117-6
Inherited conjugated hyperbilirubinemia,
1390
Inherited deficient conjugation of bilirubin as,
1389-1390
Inherited primary dystonias,
2059
Inhibin
in ovarian carcinomas,
1872t
in testicular function,
e576-4
Inhibition control,
e29-4
Initial examination of newborn,
532
Injury(ies),
333-341 See also Emergency(ies)
birth
brachial plexus palsy due to,
2383
of spine and spinal cord,
573
early childhood, foster and kinship care and,
e35-1
fire- and burn-related,
23-24
international health care and,
e61-12
international pediatric emergency medicine and,
e61-15
international prevention of,
e61-12
migraine secondary to,
2045
primary survey of,
333-337
airway/cervical spine,
335
exposure and environmental control,
337
psychological and social support for,
340
psychosocial consequences of,
25
puncture wounds of foot,
2341
secondary survey,
337-340
lower genitourinary trauma,
339
radiologic and laboratory evaluation,
340
ski- and snow board-related,
23
spinal and spinal cord,
2106
respiratory insufficiency due to,
1523
sports
differential diagnosis of,
2408
initial evaluation of,
2407
Inner ear
congenital malformations of,
e630-1
Inpatient services in international pediatric emergency medicine,
e61-15
Insect-borne infection during travel,
e168-1
Insecticides, poisoning with,
266-267
Insect repellent
for malaria prevention,
1207
for tularemia prevention,
980
Inspection in orthopedic problems,
2331,
2332t
Inspiratory flow pattern in mechanical ventilation,
327-328
Inspiratory flow waveform,
326
Inspiratory time constant in mechanical ventilation,
323
Inspiratory time in mechanical ventilation,
325-327
Inspired gas, composition of,
316
Inspissated bile syndrome,
618
Institute of Medicine (IOM)
Institutional review boards (IRBs),
e3-5-e3-6
Insulin
laboratory testing of in obesity,
185t
Insulin gene abnormalities,
1995
Insulin-like growth factor-binding protein (IGFBP),
521
Insulin-like growth factor 1 (IGF-1),
e550-1
for growth hormone deficiencies,
1881
for growth hormone excess,
e554-4
Insulin-like growth factor receptor 2 (IGF2) gene inactivation,
e486-3
Insulin lipodystrophy,
2286
Insulin pump therapy,
1977
Insulin resistance in diabetes mellitus,
1972
Insulin resistance syndrome,
e583-2
Insulin therapy
continuous subcutaneous infusion for,
1977
fear of self-injecting and self-testing in,
1986
Intellectual disability,
122-129
in Becker muscular dystrophy,
2120
diagnostic psychologic testing in,
126-127
in Duchenne muscular dystrophy,
2119
in myotonic muscular dystrophy,
2124
pathology and pathogenesis of,
124
supportive care and management of,
128-129
Intelligent quotient (IQ)
in intellectual disability,
123
Intensification treatment for acute lymphocytic leukemia,
1735
Intensity modulated radiation therapy (IMRT),
e488-5
Interactional abilities of newborn,
e7-1-e7-2
Interdisciplinary management of intellectual disability,
128
Interferons for hepatitis and human papillomavirus,
e237-5
Interferon-γ (IFN-γ)
for atopic dermatitis,
805
for chronic granulomatous disease,
746
in Rocky Mountain spotted fever,
1041
Interferon-γ receptor 1 mutations,
735
Interferon-γ receptor 2 mutations,
735
Interferon-γ release assay,
e164-4
Interferon-induced helicase gene,
1971
Interferon signature in systemic lupus erythematosus,
843
Interleukin-1 (IL-1) antagonists
for juvenile idiopathic arthritis,
838t
Interleukin-1 (IL-1) receptor, type 1 diabetes mellitus and,
1971
Interleukin-1 (IL-1) receptor antagonists, deficiency of,
858
Interleukin-2 (IL-2) receptor
type 1 diabetes mellitus and,
1971
Interleukin-2 (IL-2) receptor antibodies, in renal transplantation,
e530-3-e530-4
Interleukin-4 (IL-4)
in atopic dermatitis,
802
Interleukin-6 (IL-6), sudden infant death syndrome and,
1427
Interleukin-6 (IL-6) antagonist, for rheumatic disease,
e148-6
Interleukin-7(IL-7) Rα deficiency,
732
Interleukin-12 (IL-12)
for allergic disease,
773
Interleukin-12 (IL-12) receptor β1 mutation,
735
Interleukin-13 (IL-13)
in atopic dermatitis,
802
Interleukins (ILs),
e117-1
interaction with other immune cells,
e117-5
in systemic lupus erythematosus,
843
Interleukin-1R-associated kinase 4 (IRAK4) deficiency,
735-736
Intermittent allergic rhinitis (IAR),
775
Intermittent mandatory ventilation (IMV),
324,
324f
Internal femoral torsion,
2347
Internal jugular vein, venous access in,
295f
Internal tibial torsion,
2347
International Association for Medical Assistance to Travelers,
e168-1
International conventions for protection of children from effects of war,
e36-6
International efforts for quality improvement,
e2-7-e2-8
International immunization practices,
893-895
International League of Association for Rheumatology (ILAR),
829,
830t
International Neuroblastoma Staging System,
1755t,
1756
International normalized ratio (INR),
1696
International pediatric emergency medicine (IPEM),
278,
e61-12
continuum of care model in,
e61-12
professional organizations for,
e61-12t
quality of care improvement in,
e61-16
research collaborations in,
e61-12t
Internet
resources on,
11
for genetic disorders,
380t
for pharmacogenetics and pharmacogenomics,
e56-7t
Internuclear ophthalmoplegia in neurologic examination,
e584-4
Interstitial compartment, pulmonary edema and,
1468
Interstitial cystitis,
1830
Interstitial keratitis,
e619-3
Interstitial pneumonia
lymphocytic, HIV-related,
1165
in lysinuric protein intolerance,
455
Intervertebral disk herniation,
2377
Intervertebral disk space infection,
2376t
Interviewing
for attention deficit/hyperactivity disorder,
109-110
Intestinal disorders
acute appendicitis as,
1349-1355
differential diagnosis of,
1353
physical examination in,
1350
anorectal,
1355-1362
pilonidal sinus and abscess as,
1362
rectal mucosal prolapse as,
1361
eosinophilic gastroenteritis as,
1304
in immigrant children,
133
inguinal hernia as,
1362-1368
clinical presentation of,
1364
complications after surgical repair of,
1367-1368
malabsorption as,
1305t,
e330-1-e330-9
due to immunoproliferative small intestinal disease,
1314-1315
due to intestinal infections and infestations,
1313
due to intestinal mucosal disorders,
1308
due to liver and biliary disorders,
1318
due to malnutrition,
1315
rare inborn defects causing,
1317
Meckel diverticulum and other remnants of omphalomesenteric duct as,
1281-1282,
1282f
Intestinal epithelial dysplasia,
1341
Intestinal failure (IF), transplantation for,
e331-1t
Intestinal lymphangiectasia,
1311
Intestinal mucosal disorders,
1308
Intestinal myopathy,
1283
Intestinal neuropathy,
1283
Intestinal obstruction
See Ileus
Intracranial pressure (ICP),
296
increased,
297
migraine secondary to,
2046
Intraluminal impedance,
e310-3
in gastroesophageal reflux disease,
1267
Intramembranous ossification,
e664-1
Intramuscular (IM) drug administration,
e57-11
Intramuscular (IM) epinephrine for anaphylaxis,
817
Intramuscular immunoglobulin (IMIG),
882,
882t
Intraoral dental radiographs,
1261
Intraosseous (IO) access for emergencies,
292,
296f,
336
Intrapulmonary sequestration,
1466
Intrathecal analgesia,
373
Intrathoracic-extrapulmonary airway,
e365-5
Intrauterine devices (IUDs),
695t,
699
for special needs girls,
1875
Intrauterine growth restriction (IUGR),
555-564
definitions associated with,
555
gestational age at birth assessment in,
557,
558f
type 2 diabetes mellitus and,
1990
Intravascular access device, infections associated with,
e172-1-e172-2
Intravascular stent,
1548,
1548f
for coarctation of the aorta,
1569
Intravenous immunoglobulin (IVIG),
882,
882t
for cytomegalovirus prophylaxis,
1117
for erythroblastosis fetalis,
618
for idiopathic thrombocytopenic purpura,
1717
for myasthenia gravis,
2135
for urticaria and angioedema,
815t
Intravenous (IV) drug administration,
e57-11
Intravenous (IV) maintenance solutions,
243,
243t
for office emergencies,
e61-2t
Intravenous regional block (IVRA),
372
Intrinsic factor (IF),
1320
Intrinsic renal acute renal failure,
1819
Intrusion injury, dental,
1259
Intubation
endotracheal
for asthma exacerbation,
800
for congenital diaphragmatic hernia,
595
for infectious acute upper airway obstruction,
1448
manual ventilation before and after,
320-321
medications for placement of tube in,
321t
for respiratory distress and failure,
320
selection of tube for,
285
size and depth dimensions of tube for,
320t
In utero positioning, orthopedic problems and,
e664-1
Involuntary movement assessment in neurologic examination,
e584-7
Iodide(s)
defects of transport of,
1896
Iodine,
e51-1t
hypothyroidism due to exposure to,
1897
radioactive for Graves disease,
1912t
Iodine-deficiency endemic goiter,
1897
Iodine-deficiency goiter and cretinism,
1906-1908
Iodine-123 meta-iodobenzylguanidine (I231-MIBG) studies,
1754-1756
Iodoquinol
for infectious diarrhea,
1337t
Ion channels
strokelike events
versus mutations of,
2086
Ion transporters, skeletal dysplasias involving,
2430-2431
Ipratropium bromide
for allergic disease,
770
Irbesartan for systemic hypertension,
1645t
Iris
neurologic examination of,
e584-4
Iron
in malnutrition with chronic diarrhea,
1343t
vegetarian diets and,
168
Iron-deficiency anemia,
1655-1658
with celiac disease,
1309
clinical manifestations of,
1656
Iron overload
in sickle cell disease,
1667
Iron storage disease, neonatal,
1383,
1393
Irrigation
whole-bowel for poisoning,
257
Irritability in newborn,
e92-2
Irritable bowel syndrome (IBS),
1348-1349
chronic diarrhea with,
1341
Irritant contact dermatitis,
2250
Irritant receptors in respiration regulation,
e365-13
Irritants, avoidance of in atopic dermatitis,
806
Ischemia, due to drowning,
343
Isoflurane for anesthesia,
e70-6
Isolation techniques
in viral infection diagnosis,
e164-4
Isoleucine, defects in metabolism of,
430-438
Isopropyl alcohol poisoning,
267-268
Isovolumic hyponatremia,
218
Isoxazole intoxication,
e703-2
Isradipine for systemic hypertension,
1645t
Itraconazole,
e225-1t,
e225-2
for chronic granulomatous disease,
746
for coccidioidomycosis,
1067
for
Cryptococcus neoformans,
1058
for
Paracoccidioides brasiliensis,
e233-1
L
Labetalol
for hypertensive emergencies,
1646t
for systemic hypertension,
1645t
Labor
history of in neurologic evaluation,
e584-1
premature
group B streptococci prophylaxis in,
640f
Laboratory geneticist,
382t
Lacrimal apparatus, examination of,
2150
Lactate dehydrogenase (LDL)
in congenital dyserythropoietic anemia,
e446-1t
in ovarian carcinomas,
1872t
Lactic acidosis,
232
in type I glycogen storage disease,
492-493
Lactobacillus rhamnosus
for atopic dermatitis,
805
for functional abdominal pain,
1348t
Lactose, resumption of intake following gastroenteritis,
1336
Lactose intolerance
chronic diarrhea with,
1341
Lactulose
for constipation in palliative care,
155t-156t
for constipation maintenance therapy,
74t
for fecal disimpaction,
74t
Lafora body disease,
2024
Lambert-Eaton myasthenia gravis (LEMS),
2133t
Lamotrigine
for mood stabilization,
64t
for neuropathic pain,
368t
for seizures
adverse effects of,
2031t
Lancefield carbohydrate C,
910
Landouzy-Dejerine disease,
2126
Landry ascending paralysis,
2143
Langer-Giedion syndrome,
408t
Langerhans cell histiocytosis (LCH),
1773-1774
diabetes insipidus with,
1883
Language
chronically ill child and,
e39-3
cultural skill by health care worker and,
e4-4
development of,
115t
during first 2 years,
27t
in foreign-born adoptee,
131
during preschool years,
34
elementary school success and,
37t
Language disorders
in Asperger’s syndrome,
118
in autism and pervasive developmental disorders,
118
due to cleft lip and palate,
1253
clinical manifestations of,
117
comorbid psychiatric disorders,
121
dysfluency (stuttering, stammering) as,
122,
122t
isolated expressive language disorder as,
118
in mental retardation,
118
as neurodevelopmental dysfunction,
e29-2
pragmatic language disorder as,
118
specific language impairment as,
117-118
due to velopharyngeal dysfunction,
1253
Lansoprazole
CYP2C19 gene in metabolism of,
e56-7
for
Helicobacter pylori gastritis,
1293t
Laparoscopic surgery
in contralateral inguinal exploration,
1366,
1367f
for inguinal hernia,
1366
Laryngeal actinomycosis,
e182-2
Laryngeal cleft, posterior,
1452
Laryngeal foreign body,
1454
Laryngeal swelling, allergic,
1448
Laryngospasm during induction of anesthesia,
e70-8
Laryngotracheobronchoscopy,
1267
Laryngotracheoesophageal cleft (LTEC),
1263,
1452
Laser therapy for skin disorders,
2218
Late adolescence, growth and development during,
654
Latent tuberculosis infection (LTBI),
996-997
Late-onset central hypoventilation syndrome with hypothalamic dysfunction (LO-CHS),
1521-1522
Lateral epicondylitis,
2411
Lateral penile curvature,
1857
Lateral pivot shift test,
2415f
Latex agglutination (LA) test,
e164-1
Latex allergy
anaphylactic reaction to,
816,
816t
neuropathic bladder and,
e536-3
Latino population
disease beliefs or practices of,
e4-2t
as special needs population,
7
Latrodectus antivenin,
258t
Laundry, infection protection and control and,
e166-2t
Lavandula for sedation,
271t
Lavender for sedation,
271t
Lead exposure/poisoning,
e700-2
δ-aminolevulinic acid dehydratase deficiency due to,
e85-4
clinical effects of,
2450
intellectual disability and,
127t
Lead mobilization test,
2451
Learning disorders,
e29-1 See also Neurodevelopmental dysfunction
attention deficit/hyperactivity disorder as,
108
clinical manifestations of,
108-109
intellectual disability as,
122-129
diagnostic psychologic testing in,
126-127
pathology and pathogenesis of,
124
supportive care and management of,
128-129
language and communication disorders as,
114-122
in Asperger’s syndrome,
118
in autism and pervasive developmental disorders,
118
clinical manifestations of,
117
comorbid psychiatric disorders,
121
dysfluency (stuttering, stammering) as,
122,
122t
isolated expressive language disorder as,
118
in mental retardation,
118
pragmatic language disorder as,
118
specific language impairment as,
117-118
neurodevelopmental dysfunction as,
e29-1-e29-9
assessment and diagnosis of,
e29-7
executive functioning,
e29-4
neuroacademic problems,
e29-7
spelling and writing impairments,
e29-6
terminology and epidemiology of,
e29-1
Leber congenital retinal amaurosis (LCA),
2177
Lecithin, amniotic fluid,
548
Lecithin-cholesterol acyltransferase (LCAT) deficiency,
477
Lecithin-sphingomyelin (L:S) ratio,
548-549
Leflunomide
for juvenile idiopathic arthritis,
838t
Left-to-right-shunt
in neonatal circulation,
e415-2
Left ventricle
hypertrophy of
systemic hypertension with,
1642
Left ventricular assist device (LVAD),
1638
Legislation
foster and kinship care,
e35-1
Registration, Evaluation, Authorization, and restriction to Chemicals (REACH),
e700-1
Leishmaniasis,
1186-1190
differential diagnosis of,
1189
laboratory findings in,
1189
predisposition to due to immunodeficiency,
716t
Leisure and recreational activities in intellectual disability management,
128-129
Lemon balm for sedation,
271t
Lenalidomide for rheumatic disease,
e148-6
Lentiginosis profusa,
2236
LEOPARD syndrome
cardiac manifestations of,
1531t
Lepromatous leprosy (LL),
e208-1
Leptin deficiency, obesity due to,
182t
Leptin receptor gene deficiency, obesity due to,
182t
Leptospira interrogans,
1023
Leptospiruric leptospirosis,
1024
Leri-Weil dyschondrosteosis,
388-389
Lethal spondyloepiphyseal dysplasias,
2424,
2424f
Lethal toxic encephalopathy,
960
Leucine, defects in metabolism of,
430-438
Leucine-sensitive hypoglycemia,
525
Leukemia,
1732-1739
acute lymphocytic,
1732-1737
differential diagnosis of,
1734
hematopoietic stem cell transplantation for,
757,
758f
incidence and survival rates for,
1726t
secondary, due to radiation therapy,
e699-5t
supportive care for,
1736
chromosomal translocation of,
e486-1
chronic myelogenous,
748t,
1738-1739
hematopoietic stem cell transplantation for,
758
environmental carcinogens and,
e700-3
juvenile idiopathic arthritis
versus,
835
juvenile myelomonocytic,
1739
hematopoietic stem cell transplantation for,
758
Leukocystoclastic vasculitis,
868t
Leukocytes
cerebrospinal fluid in CNS infection,
2088t
fecal in chronic diarrhea,
1344t
Leukocytoclastic vasculitis,
876
due to cat-scratch disease,
985
Leukocytosis,
e126-1-e126-3
in eosinophilic pustular folliculitis,
2220
in Epstein-Barr virus infection,
1113
in hantavirus pulmonary syndrome,
e265-1
Leukokoria in newborn,
534
Leukomalacia, periventricular,
566-568
optic nerve hypoplasia with,
e623-1
Leukoplakia, oral hairy,
2299
Leukorrhea, physiologic,
1866
Leukotriene-modifying agents (LTRAs)
for allergic disease,
772
for urticaria and angioedema,
815t
Leukovorin for toxoplasmosis,
1215
Leuprolide
for precocious puberty,
1889
for premenstrual dysphoric disorder,
692t
Levamisole for nephrotic syndrome,
1805
Level of consciousness (LOC) in hypoxic-ischemic encephalopathy,
571t
Levetiracetam
adverse effects of,
2031t
for migraine prophylaxis,
2044t
Levocabastine for allergic conjunctivitis,
811t
Levodopa for spasticity of cerebral palsy,
2064
Levorphanol for neuropathic pain,
368t
Levothyroxine for hypothyroidism,
1900,
1903
Leydig cell aplasia,
1964
Leydig cell tumor, testicular,
1950
Licensing, child care,
e15-1
Lichenoid eruption in graft
versus host disease,
e637-6f
Licorice for asthma,
271t
Lidocaine
for pediatric resuscitation and arrhythmias,
294t
in rapid sequence intubation,
287t
Life course-limited offenders,
669
Lifestyle
type 2 diabetes mellitus and,
1991
Life-sustaining medical treatment (LSMT)
withholding and withdrawing of,
e3-2
Light sensitivity in migraine,
2041
Lily of the valley toxicity,
269t
Limb-body wall complex (LBWC),
2221
Limp
of Legg-Calvé-Perthes disease,
2361
Linear immunoglobulin A dermatosis,
2249,
2249f
Linear nevus syndrome,
2052
Linear nondose threshold (LNT),
2448
Linens, infection protection and control and,
e166-2t
Lingual frenulum, short,
1240
Linguistic development
during preschool years,
34
Linoleic acid (LA),
e41-15
deficiency, cutaneous manifestations of,
2329
Lip
assessment of in allergic disease,
765
Lipids
cardiovascular disease and,
470
storage disorders of,
484t
Lipidoses,
482-491,
483f,
486f
cholesterol ester storage disease as,
491
clinical findings in,
484t
metachromatic leukodystrophy as,
490
multiple sulfatase deficiency as,
490
Niemann-Pick disease as,
488
Schindler disease as,
490
Lipoatrophic diabetes,
1995
Lipoid adrenal hypoplasia,
1925t
Lipoproteins
cardiovascular disease and,
470
high-density,
471,
472f,
472t,
479t
disorders of metabolism of,
477
reverse cholesterol transport and,
473
patterns of in children and adolescents,
479,
479t
Liposomal amphotericin B,
1053
5-Lipoxygenase inhibitor for asthma,
794t
Lisinopril for systemic hypertension,
1645t
Lithium carbonate, goiter due to,
1908
Lithium for mood stabilization,
63,
64t
Live-attenuated influenza vaccine (LAIV),
883-884,
884t
Liver
fatty
with type 2 diabetes mellitus,
1993t
insulin level effects on,
1975t
newborn assessment of,
535
porphyria cutanea tarda and,
e85-11
shock-related dysfunction of,
307t
Liver disease
chronic diarrhea with,
1341
glycogen storage disease as,
492-499
hemolytic anemia secondary to,
e459-1
hemorrhagic disorders due to,
1712
due to intestinal failure,
e331-1
malabsorption due to,
1318
metabolic,
1388-1393,
1389t
α-antitrypsin deficiency,
1393
Indian childhood cirrhosis,
1392
inherited deficient conjugation of bilirubin as,
1389-1390
neonatal iron storage disease as,
1393
psychopharmacology and,
64-65
pulmonary manifestations of,
e413-1t
Liver-kidney microsomal (LKM) antibody,
1409
Liver phosphorylase deficiency,
497
Liver phosphorylase kinase deficiency,
498
Liver transplantation,
e360-1-e360-2
for acute liver failure,
1414
for type I glycogen storage disease,
495
Liver tumor
precocious puberty due to,
1891
Lobelia inflata, potential toxicity of,
272t-273t
Lobular capillary hemangioma,
2229
Local anesthesia
toxicity, neonatal seizures due to,
2034,
2036
Localized cutaneous leishmaniasis (LCL),
1187-1188
Locus heterogeneity,
e77-2
Lodoxamide tromethamine
for allergic conjunctivitis,
811t
for allergic disease,
772
Logical thinking in adolescent,
649-651
Logistic access in chronic illness,
e39-3
Long-acting inhaled β-adrenergic agents (LABAs)
for allergic disease,
770
Long-chain fatty acid transporter deficiency,
457t
Long-chain 3-hydroxyacyl CoA dehydrogenase (LCHAD) deficiency,
457t,
460
Longdan xieganwan, potential toxicity of,
272t-273t
Longitudinal vaginal septa,
e548-4
Long terminal repeats,
1157
Long-term memory (LTM),
e29-3
Long-term survivors (LTSs), HIV,
1161
Long-term video electroencephalography monitoring,
e584-10
Loop diuretics, metabolic alkalosis due to,
236
Loose folds of skin,
2220
Loperamide
for infectious diarrhea,
1337
for traveler’s diarrhea,
e168-5
Loratadine
for urticaria and angioedema,
815t
Lorazepam
for cyclic vomiting syndrome,
1244t
for depression and anxiety symptoms,
63t
for hypoxic-ischemic encephalopathy,
571
for pain management in palliative care,
155t-156t
for sleep disturbance/insomnia in palliative care,
155t-156t
Lorenzo’s oil therapy,
469
Losartan for systemic hypertension,
1645t
Lower body segment, body proportions and,
e13-4
Lower esophageal sphincter (LES),
e310-1-e310-2
gastroesophageal reflux disease and,
1266
Lower extremity(ies)
musculoskeletal pain syndrome of,
877t
septic arthritis in,
2399
Lower extremity nerve block,
372
Lower genitourinary tract trauma,
339
Lower respiratory tract infection (LRTI)
respiratory culture in,
e164-2
Low molecular weight (LMW) heparin,
1710t,
1711
for pulmonary embolism,
1502
Lubricants for skin disorders,
2216
Lumbar disk herniation, strain, and contusion,
2412
Lumbar sympathetic block,
373
Lumpy-bumpy deposits, glomerular,
e502-3
in acute poststreptococcal glomerulonephritis,
1783,
1783f
Lung
See also Respiratory system
auscultation of,
276
in acutely ill child evaluation,
276
maintenance water and,
244t
skeletal diseases influencing function of,
1516-1519
unilateral hyperlucent,
1461
ventilator-induced injury to,
329
Lung disease
See also Respiratory disease
abscess as,
1480-1481
clinical manifestations of,
1480
pathology and pathogenesis of,
1480
congenital,
1463-1467
agenesis and aplasia as,
1463
bronchobiliary fistula as,
1467
cystic adenomatoid malformation as,
1464,
1465f
lymphangiectasia as,
1467
failure to thrive in,
148t
parenchymal
emergency airway management in,
284
respiratory acidosis due to,
239,
239t
respiratory alkalosis and,
241
Lung infiltrates
in acute lung injury,
317f
Lung manifestations
in Niemann-Pick disease,
488
in systemic inflammatory response syndrome,
309t
in systemic lupus erythematosus,
843t
in systemic scleroderma,
851
Lung sounds
in acutely ill child evaluation,
276
Lupus erythematosus (LE)
cutaneous manifestations of,
e637-3
Lupus erythematosus panniculitis,
2283,
2283f
Luteinizing hormone (LH),
e550-2
in precocious puberty,
1888
in testicular function,
e576-1
Luteinizing hormone-releasing hormone (LHRH),
1860
17,20 Lyase deficiency,
1964
Lyme disease,
1025-1029
juvenile idiopathic arthritis
versus,
835
pathology and pathogenesis of,
1026
Lymphangiectasia,
1724
congenital pulmonary,
1467
Lymphangioma circumscriptum,
1724
Lymphatic compartment, pulmonary edema and,
1468
Lymphatic dysplasia,
1724
Lymphatic system
anatomy and function of,
e482-1
in total body water regulation,
e52-1
Lymph node disease
Cryptococcus neoformans infection as,
1057
Lymph node syndrome, mucocutaneous,
862-867
Lymphocyte blastogenesis to
Toxoplasmosis antigens,
1214
Lymphocyte count
in adenosine deaminase deficiency,
732
in severe combined immunodeficiency,
731
whole-body irradiation and,
e699-6t
Lymphocytic interstitial pneumonia (LIP),
1165
Lymphocytic thyroiditis,
1903-1905
type 1 diabetes mellitus with,
1996
Lymphogranuloma venereum (LGV),
1038
Lymphohematogenous (disseminated) tuberculosis,
1004
Lymphoid hypoplasia in X-linked agammaglobulinemia,
724
Lymphoid organs, development of,
e117-6
Lymphoid tyrosine phosphatase (SNP),
1971
Lymphoma,
1739-1746
of gastrointestinal tract,
e337-3
late effects in children and adolescents with,
1746
mucosa associated lymphoid tissue,
1315
primary effusion based,
1121
Lymphopenia,
752,
752t
in adenosine deaminase deficiency,
732
due to ehrlichiosis,
1049
in severe combined immunodeficiency,
731
Lymphoproliferation, human T-lymphocyte-associated,
e269-1
Lymphoproliferative disease,
721t
X-linked,
727
Epstein-Barr virus and,
1112
Lysergic acid diethylamide (LSD),
682
Lysinuric protein intolerance (LPI),
455,
1320
Lysosomal acid α-1,4-glucosidase deficiency,
499-500,
500f
Lysosomal-associated membrane protein 2 (LAMP2) deficiency,
500
Lysosomal storage disorders,
482-491,
483f,
486f
cholesterol ester storage disease as,
491
clinical findings in,
484t
genetic therapies for,
381
metachromatic leukodystrophy as,
490
multiple sulfatase deficiency as,
490
Niemann-Pick disease as,
488
Schindler disease as,
490
Lysyl hydroxylase deficiency,
2278
M
Machado-Joseph disease (MJD),
2057t
Macroadenoma, insulin-secreting,
522-523
Macrocephaly
in Tay-Sachs disease,
485
Macrophage-colony-stimulating factor (M-CSF), fetal,
e440-1,
e440-1t
Macrosomia in persistent hyperinsulinemic hypoglycemia,
522t
Macular red cherry spot,
483
Macule, examination of,
2215
Mafenide acetate for burn injury,
353,
353t
Magnesium sulfate for pediatric resuscitation and arrhythmias,
294t
Magnetic resonance angiography (MRA)
in attention deficit/hyperactivity disorder,
e30-1
computer processing of,
1546
in orthopedic problems,
2335
in septic arthritis,
2400
Magnetic resonance cholangiography (MRC),
e352-1
Magnetic resonance imaging (MRI)
in fever of unknown origin,
902
functional in neurologic examination,
e584-11
in juvenile idiopathic arthritis,
837f
of müllerian anomalies,
e548-1
in X-linked adrenoleukodystrophy,
468,
469f
Magnetic resonance spectroscopy (MRS),
1545-1546
Magnetic resonance venography (MRV),
e584-11
Maintenance of Certification (MOC),
e2-2-e2-3
Maintenance therapy,
242,
242t
intravenous solutions for,
243,
243t
selection of solutions for,
243
Major aortopulmonary collateral arteries (MAPCAs),
1573-1575,
1578
Major basic protein (MBP), neutrophil,
739
Major histocompatibility complex (MHC),
e117-4-e117-5
defective expression of,
734
type 1 diabetes mellitus and,
1970
Major outer membrane protein (MOMP),
1033-1034
Malabsorption,
1305t,
e330-1-e330-9
due to immunoproliferative small intestinal disease,
1314-1315
due to intestinal infections and infestations,
1313
due to intestinal mucosal disorders,
1308
due to liver and biliary disorders,
1318
due to malnutrition,
1315
rare inborn defects causing,
1317
Malaria,
1198-1207
differential diagnosis of,
1202
predisposition to due to immunodeficiency,
716t
returning traveler with fever and,
e168-7
Malar rash
of systemic lupus erythematosus,
e637-4f
Male fertility, inguinal hernia repair and,
1368
Malignancy
brain tumors as,
1746-1753
clinical manifestations of,
1747
complications and long-term management of,
1753
craniopharyngioma as,
1752
Candida infections with,
1055
as complication of enterocystoplasty,
e536-2
cutaneous manifestations of,
e637-6
desmoplastic small round cell tumor as,
1773
fever without a focus in,
896t
hepatocellular,
1772
in type II glycogen storage disease,
496
hypercalcemia due to,
1922
impact of cancer therapy on fertility and,
1870-1871
incidence rates for,
1727f
lymphoma as,
1739-1746
of gastrointestinal tract,
e337-3
late effects in children and adolescents with,
1746
medullary, diarrhea caused by,
e333-2t
pulmonary embolism with,
1500
secondary,
e488-9
after hematopoietic stem cell transplantation,
e133-1
“two-hit” model of development of,
e486-1
Malignant external otitis,
2197
Malignant melanoma, maternal,
e89-2t
Mallet finger deformity,
2391
Mallory-Weiss tear,
1243t
Malnutrition,
170
with chronic diarrhea,
1343t
common causes of in early life,
148t
malabsorption due to,
1315
Malone antegrade continence enema procedure,
e536-2
Mandible, hypoplasia of, as delivery room emergency,
575
Mandibulofacial dysostosis,
1254
Mania
psychopharmacologic management of,
61t
Mannan-binding lectin-associated serine protease 2 (MASP-2) deficiency,
754-755,
754t
Mannitol for acute renal failure,
1820
Manometry
anorectal
in congenital intestinal pseudo-obstruction,
1283t
in Hirschsprung disease,
1286
antroduodenal in congenital intestinal pseudo-obstruction,
1283t
Mantoux tuberculin skin test,
1001
Maple syrup urine disease (MSUD),
430-438
neonatal seizures due to,
2036
Marasmic kwashiorkor,
175
Marcus Gunn jaw-winking ptosis,
2163
Marcus Gunn phenomenon,
2006
Marden-Walker syndrome,
2138
Marfan syndrome (MFS),
2440-2446
current and future therapies for,
2445
diagnostic criteria for,
2442t
family and genetic history in,
2443
genetic counseling in,
2446
laboratory findings in,
2444
Marnier-Kuhn syndrome,
1479
Mask
oxygen administration through,
319
Masquerade syndromes,
2174
Mass(es)
abdominal,
1249
in newborn assessment,
535
nondigestive causes of,
1241t
Mastocytoma, diarrhea caused by,
e333-2t
Masturbation, seizure
versus,
e587-4
Maternal factors
in attention deficit/hyperactivity disorder,
108
for sudden infant death syndrome,
1424
Maternal interests, fetal interests
versus,
e3-6
Maternally inherited diabetes and deafness (MIDD),
1994-1995
Maternal phenylketonuria (PKU),
e89-2t
congenital heart disease with,
1531t
Maternal radiation exposure,
e699-2
Maternal serum α-fetoprotein concentration,
543t
Maternal substance abuse
sudden infant death syndrome and,
1424
Maternal thyroiditis, postpartum,
1904t
Maximal midexpiratory flow rate,
e366-3
Maximum forced expiratory flow (FEF max),
1419,
e365-2f
Maximum urine osmolality,
e52-4
Mayer-Rokitansky-Küster-Hauser syndrome (MRKH),
1827,
e548-4
McKusick Metaphyseal chondrodysplasia,
2434
Mead Johnson bottle,
1253
Mean arterial pressure (MAP),
311t
Mean corpuscular hemoglobin concentration (MCHC), reference values for,
e708-2t-e708-8t
Mean corpuscular volume (MCV)
Measles,
1069-1075
differential diagnosis of,
1071
exclusion from day care due to,
e15-2t
in immigrant children,
134
laboratory findings in,
1071
Measles, mumps, rubella, varicella (MMRV) vaccine,
884t,
1078
Measurements in growth assessment, accurate,
e13-1
Mechanical ventilation,
321-329,
321f-322f
airway pressure release,
326
assist control mode in,
324
for asthma exacerbation,
800
for congenital diaphragmatic hernia,
595
conventional settings for,
327
expiratory phase maneuvers in,
326
functional residual capacity in,
322,
323f
initiation of inspiration in,
324
inspiratory phase characteristics in,
325-326
intermittent mandatory ventilation mode in,
324,
324f
patient-ventilator asynchrony in,
327-328
for persistent pulmonary hypertension of the newborn,
593
in pertussis management,
947
PHOX2B gene and dependence on,
1520
for respiratory distress syndrome,
584-585
termination of inspiration cycle in,
326
Meckel-Gruber syndrome,
1531t
Meconium peritonitis,
601
in cystic fibrosis,
1487f
Meconium staining,
577
high-risk infant due to,
552
in hypoxic-ischemic encephalopathy,
570
Media, radiocontrast, adverse reaction to,
828
Media coverage of war,
e36-6
Medial collateral ligament (MCL) injury,
2414
Median cubital vein, venous access in,
292,
295f
Mediastinal “crunch”,
1512
Mediastinal disease in Hodgkin lymphoma,
1741,
1742f
Mediastinum, air or gas in,
1512
Medical biochemical geneticist,
382t
Medical care
coordination of for foster care children,
e35-2t
Medical control physician (MCP),
e61-7
Medical home, chronic illness and,
e39-2
Medical profession, culture of,
e4-3
Medical records
preadoption review of,
130
Mediterranean lymphoma of small intestine,
1314-1315
Medium-chain acyl CoA dehydrogenase (MCAD) deficiency,
457t,
459-460
Medroxyprogesterone acetate,
697-698
Medullary carcinoma, diarrhea caused by,
e333-2t
Medullary cystic kidney disease complex (MCKD),
1816
Medullary sponge kidney,
1810
Megaesophagus in Chagas disease,
1196
Megestrol acetate for anorexia in palliative care,
155t-156t
Melanoblast migration abnormalities,
2239-2240
Melanocortin 4 receptor gene deficiency,
182t
Melatonin for delayed sleep phase disorder,
53-54
Melissa officinalis for sedation,
271t
Meloxicam
for juvenile idiopathic arthritis,
838t
Membrane cofactor protein,
1792t
Membrane complement control protein deficiency,
755
Membranous conjunctivitis,
2168
Meningitis
bacterial,
2087-2095
cerebrospinal fluid findings in,
2088t
clinical manifestations of,
2090
Haemophilus influenzae type b in,
2089
pathology and pathophysiology of,
2089
Streptococcus pneumoniae in,
2087
cerebrospinal fluid findings in,
2088t
as cerebrospinal fluid shunt infection,
e172-2
Cryptococcus neoformans in,
1057
group B streptococcal,
927
herpes simplex virus,
1101
Listeria monocytogenes,
e181-2
Pseudomonas aeruginosa in,
977
Staphylococcus aureus in,
905
Meningococcal conjugate vaccine (MCV),
884t
recommended schedule for,
887f,
889
for special circumstances,
889
Meningococcus,
929-935
differential diagnosis of,
932
Meningoencephalitis
due to human monocytic ehrlichiosis,
1049
Menkes kinky hair syndrome,
2292
Mental health action signs,
57,
57t
Mental health services
minors right to consent for,
e106-2
referral to for eating disorders,
95-96
Mental status
of acutely ill child,
275
bacterial meningitis and,
2090
effects of eating disorders on,
93t
evaluation of,
e584-2
in psychiatric diagnostic evaluation,
60
Mentha pulegium, potential toxicity of,
272t-273t
Meperidine
for cyclic vomiting syndrome,
1244t
equianalgesic doses and half-life of,
367t
for pain management,
365t
6-Mercaptopurine
for autoimmune hepatitis,
1410
Merkel cell polyomavirus,
1157
Mesangial proliferation in idiopathic nephrotic syndrome,
1804
Mesenteric arteritis, postoperative,
1569
Mesial temporal sclerosis,
2023
Mesoblastic nephroma,
1760
Messenger DNA in sudden infant death syndrome,
1427
Metabolic acidosis,
230t,
231-235
in chronic kidney disease,
1824
clinical manifestations of,
233
as complication of enterocystoplasty,
e536-2
hypophosphatemia and,
227
in respiratory distress syndrome,
586
in tetralogy of Fallot,
1574
Metabolic bone disease
primary chondrodystrophy (metaphyseal dysplasia) as,
e695-1,
e695-1f
Metabolic disorders,
416-418,
417f,
418t
of amino acids,
418-456
malabsorption due to,
1318
of valine, leucine, isoleucine, and related organic acidemias,
430-438,
430f
failure to thrive in,
148t
hypoglycemia as,
517-531
diagnosis and differential diagnosis of,
524t,
530
significance and sequelae of,
517-518
language disorders due to,
119
of liver,
1388-1393,
1389t
α-antitrypsin deficiency,
1393
Indian childhood cirrhosis,
1392
inherited deficient conjugation of bilirubin as,
1389-1390
neonatal iron storage disease as,
1393
multiple organ dysfunction syndrome and,
312t
physiologic therapies for,
379
in premature infants,
559t
respiratory distress due to,
315t,
316
severe intellectual disability in,
123t
strokelike events
versus,
2086
systemic inflammatory response syndrome and,
309t
Metabolic disturbances
in newborn,
418-456
metabolic bone disease as,
623
due to selective serotonin reuptake inhibitors,
625,
625f
Metabolism
effects of eating disorders on,
93t
effects of vomiting on,
1243t
Metacarpal bones, centers of ossification appearance in,
29t
Metacyclic trypomastigotes,
1193f
Metalinguistic difficulties,
e29-2
Metalloporphyrins for hyperbilirubinemia,
612
Metal metabolism, defects of,
1389t
Metanephrines
in neuroendocrine tumor-associated diarrhea,
e333-2t
in pheochromocytoma,
1942
Metaphyseal chondrodysplasia
Metaphyseal fracture, due to child abuse,
138,
139f
Metastatic Crohn disease,
e637-4
Metatarsal fracture,
2393
Metered-dose inhaler (MDI),
e57-11
Methacholine challenge testing,
768
Methadone
equianalgesic doses and half-life of,
367t
maternal addiction to,
624
for pain management,
365t
Methemoglobinemia
respiratory signs and symptoms of,
e413-1t
Methicillin-resistant
Staphylococcus aureus (MRSA),
907t
Methicillin-susceptible
Staphylococcus aureus (MSSA),
906-907,
907t
Methotrexate (MTX)
for atopic dermatitis,
805
for juvenile dermatomyositis,
849
for juvenile idiopathic arthritis,
837,
838t
2-Methylacyl CoA racemase deficiency,
465,
466t
Methylcobalamin, homocystinuria due to defects of,
427,
428f
Methylcobalamin deficiency,
e448-5
3-Methylcrotonyl CoA carboxylase deficiency,
433
Methyldopa for systemic hypertension,
1645t
Methylenedioxymethamphetamine (MDMA),
675t,
682
Methylenetetrahydrofolate reductase (MTHFR) deficiency,
427
3-Methylglutaconic aciduria,
433
3-Methylglutaconyl CoA hydratase deficiency,
433
Methylphenidate
for attention deficit/hyperactivity disorder,
62t,
111t
Methylprednisolone
for juvenile dermatomyositis,
849
for multiple sclerosis,
2077
for systemic lupus erythematosus,
844
Methyl salicylate toxicity,
251t
Metoclopramide
for chemotherapy-associated vomiting,
1244t
Metoprolol
for systemic hypertension,
1645t
Mexiletine
for neuropathic pain,
368t
Michelis-Castrillo syndrome,
e52-10
Microadenoma in hyperinsulinemia,
521-522
Microalbuminuria,
1800
with type 2 diabetes mellitus,
1993t
Microdeletion syndrome,
396
Micrognathia in juvenile idiopathic arthritis,
832
Microimmunofluorescence (MIF)
Micronutrients
management of in protein-energy malnutrition,
178t
supplementation for chronic diarrhea,
1345
Microphthalmia with linear defects (MLS),
408t
Microscopy in bacterial and fungal infection diagnosis,
e164-1,
e164-1t
Midazolam
for neonatal seizures,
2037
Middle adolescence, growth and development during,
653-654
Middle ear
congenital malformations of,
e630-1
Middle-ear effusion (MEE),
2199-2200
acute otitis media
versus otitis media with effusion and,
2203-2204
Midline nasal masses, congenital,
1431,
1431f
Mid-upper arm circumference (MUAC), in nutrition assessment,
172
Midureteral obstruction,
1842
Migrant children,
7
effects of relocation on,
e16-2
Migrant Health Program,
10
Migratory polyarthritis in acute rheumatic fever,
921-922
Milk
cow’s
type 1 diabetes mellitus and,
1972
human
protective effects of,
161t
Milk of magnesia
for constipation maintenance therapy,
74t
for fecal disimpaction,
74t
Milk of molasses enema,
74t
Millard rotation-advancement technique,
1252-1253
Millennium Development Goals (MDGs),
1,
173-174
Miller-Dieker syndrome,
408t
Milligrams to milliequivalents per liter conversions,
e708-10t
Milrinone
for cardiac output maintenance and post-resuscitation stabilization,
294t
for cardiogenic shock,
313t
Miltefosine for leishmaniasis,
1190
Milwaukee brace
for Scheuermann disease,
2372
Mineralocorticoids
for 21-hydroxylase deficiency,
1934
Mineralocorticoid receptors in steroid hormone regulation,
e568-4
Mineral oil
for constipation maintenance therapy,
74t
for fecal disimpaction,
74t
Minerals
deficiency in metabolic bone disease,
e694-1
supplemental for cystic fibrosis,
1495
Minimal alveolar concentration (MAC), of inhalation anesthetic,
e70-5
Minimal change nephrotic syndrome (MCNS),
1803t,
1804
Minimal residual disease (MRD), acute lymphocytic leukemia,
1737
Minimum bactericidal concentration (MBC),
e164-3
Minimum inhibitory concentration (MIC),
e164-3
Minimum urine osmolality,
e52-4
Minoxidil
for hypertensive emergencies,
1646t
for systemic hypertension,
1645t
Miralax for constipation in palliative care,
155t-156t
Miscarriage, parvovirus B19 infection and,
1653
Mitochondrial acetoacetyl CoA thiolase deficiency,
433-434,
434f
Mitochondrial chromosome,
e74-1
Mitochondrial DNA depletion syndrome (MDS),
1406,
2132
Shwachman-Diamond syndrome with,
1687
Mitochondrial 3-hydroxy-3-methylglutaryl CoA synthase deficiency,
435
Mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes (MELAS),
391,
391t,
2066,
2113t,
2131
Mitochondrial trifunctional protein (TFP) deficiency,
457t,
460
Mitral valve
cleft in anterior leaflet of,
1554
coarctation with disease of,
1570
Mitral valve prolapse,
1572
Mitral valvuloplasty,
1572
Mixed amphetamine salts,
111t
Mixed connective tissue disease (MCTD),
e147-3t
Mixed venous oxygen saturation, in shock,
309-310
Mobility, tympanic membrane,
e628-2
Mobitz type 1 heart block,
1618
Model for Improvement,
e2-3f
Modified Checklist for Autism in Toddlers (M-CHAT),
41t-43t
Molding of skull, assessment of,
e584-2
Molecular defects
liver disease caused by,
1383t
in persistent hyperinsulinemic hypoglycemia,
522t
Mollaret meningitis,
1101
Molybdenum cofactor deficiency,
429,
e83-7
Monamine neurotransmitter metabolism, disorders of,
2059
Mongolian spots,
2219,
2219f
child abuse bruising
versus,
137
Monitoring, home
in mechanical ventilation,
1525
in sudden infant death syndrome prevention,
1428-1429
Monoamine oxidase inhibitors (MAOIs)
in serotonin syndrome,
265t
Monoamine oxidase (MAO) deficiency,
447
Monogenic type 1 diabetes mellitus,
1970
Monomethylhydrazine intoxication,
e703-1
Mononeuritis multiplex,
2140
Mononuclear phagocyte system,
739
Mononucleosis-like illness,
1110
Montelukast
for urticaria and angioedema,
815t
Montenegro skin test,
1187
Mood disorders,
82
dysthymic disorder as,
87,
87t
Mood stabilizers,
63,
64t
Moral development
during middle childhood,
38
during preschool years,
35-36
Morbidity(ies)
perinatal and neonatal,
e87-4t
Morning glory disc anomaly,
e623-1
Moro reflex
in hypoxic-ischemic encephalopathy,
571t
in neurologic examination,
e584-7
Morphine
equianalgesic doses and half-life of,
367t
for pain management,
365t
possible adverse reactions to in premature infant,
563t
urine screening in adolescent abuse of,
676t
Morquio-Ullrich syndrome,
1531t
Mosquitoes
in arboviral encephalitis transmission,
1141-1142
avoidance during travel,
e168-6
in dengue fever transmission,
1147
in hemorrhagic fevers transmission,
1150t
in yellow fever transmission,
e262-1
Motilin agonists for vomiting,
1244t
Motivational therapy for nocturnal incontinence,
1852
Motor apraxia, congenital ocular,
2161
Motor dysmetria, ocular,
2162
Motor vehicle injuries,
21-22,
21f,
21t
as leading cause of death,
18
Mouth-to-mouth ventilation,
282,
282f
Movements, involuntary, assessment in neurologic examination,
e584-7
Movement therapy for pain management,
371
MPL, missense mutations of,
1689
Mucocutaneous candidiasis,
1056
Mucocutaneous lymph node syndrome,
862-867
Mucosa
rectal, prolapse of,
1361
Mucosa associated lymphoid tissue (MALT) lymphoma,
1315
Müllerian duct syndrome, persistent,
1964-1965
Müllerian inhibiting substance
Multicenter Growth Center Study (MGRS),
e13-2
Multicentric Castleman disease,
1121
Multichannel intraluminal impedance (MII),
e310-3
in gastroesophageal reflux disease,
1267
Multicolor fluorescence in situ hybridization (M-FISH),
396
Multi-dose activated charcoal (MDAC),
257-258
Multiple endocrine neoplasia (MEN), type 1,
527
Zollinger-Ellison syndrome with,
1294
Multiple endocrine neoplasia (MEN), type 2A,
1916
pheochromocytoma with,
1942
Multiple endocrine neoplasia (MEN), type 2B,
1916
Multiple epiphyseal dysplasias (MED),
2427
Multiple hamartoma syndrome,
2298
Multiple physician model for emergency care,
e61-12
Multiple sulfatase deficiency,
490
Multivisceral graft in intestinal transplantation,
e331-1
Munro-Kellie doctrine,
297f
Murmur, heart
infective endocarditis and,
1623
Muscle(s)
assessment of in neurologic examination,
e584-6
brain malformations and development of,
2118
effects of malnutrition on,
175t
insulin level effects on,
1975t
mitochondrial encephalomyopathy and,
2065t
phosphorylase kinase deficiency in,
498
Staphylococcus aureus abscess in,
905
Muscle adenosine monophosphate deaminase deficiency,
e83-6-e83-7
Muscle biopsy
in Duchenne and Becker muscular dystrophy,
2120,
2120f
in myasthenia gravis,
2134
in neuromuscular disorders,
2110t
Muscle-derived enzymes in juvenile dermatomyositis,
848,
848t
Muscle-eye-brain disease of Santavuori,
2127
Muscle glycogen synthase deficiency,
498
Muscle pain in neuromuscular disorders,
2109
Muscle phosphofructokinase deficiency,
501
Muscle phosphorylase deficiency,
500-501
Muscle receptors in respiration regulation,
e365-13
Muscle relaxants
in rapid sequence intubation,
287t
Muscle rigidity assessment in neurologic examination,
e584-6
Muscle spasm, treatment of in palliative care,
155t-156t
Muscle spasticity assessment in neurologic examination,
e584-6
Muscle strength assessment in neurologic examination,
e584-6,
e584-8f
Muscle tone
assessment of
in neuromuscular disorders,
2109
in hypoxic-ischemic encephalopathy,
571t
Muscle wasting in malabsorption syndromes,
1305,
1306f
Muscle weakness
in Becker muscular dystrophy,
2119
in Duchenne muscular dystrophy,
2119
in Guillain-Barré syndrome,
2143
Muscular dysgenesis (proteus syndrome myopathy),
2119
Musculoskeletal disorders
Mutilating keratoderma,
2273
Mutism, selective,
79,
118
Myalgia in neuromuscular disorders,
2109
Mycobacterial infection
predisposition to due to immunodeficiency,
716t
Mycobacteria other than tuberculosis (MOTT),
1011-1016
Mycobacterium abscessus,
1014
in cystic fibrosis infection,
1494
Mycobacterium fortuitum group
Mycobacterium kansasii
in cutaneous infection,
2308
in cystic fibrosis infection,
1494
Mycobacterium scrofulaceum skin infection,
2308
Mycobacterium ulcerans,
1013
Mycophenolate mofetil (MMF)
for atopic dermatitis,
805
for nephrotic syndrome,
1805
in renal transplantation,
e530-4
Mycoplasmal infections
in infective endocarditis,
1624t
Mydriasis, congenital,
2155
Myelination
during age 0-2 months,
26-27
of optic nerve fibers,
2181
Myelodysplastic syndromes,
748t
hematopoietic stem cell transplantation for,
758-759
Myelogenous leukemia, chronic,
748t,
1739
hematopoietic stem cell transplantation for,
758
Myeloid cells, acquired disorders of,
747,
748t
Myeloid precursor cells, intrinsic disorders of,
747,
748t
Myelomonocytic leukemia, juvenile,
758
Myelopathy, human T-lymphotropic virus in,
e269-1
Myeloproliferative disorders, Down syndrome with,
1738
Myelosuppression, due to chemotherapy,
e488-5
Myenteric plexus neuropathies,
2143
MYH9-related thrombocytopenia,
1720
Myocardial biopsy in heart transplantation monitoring,
e437-2
Myoclonic astatic epilepsy,
2024
Myoclonic seizure, neonatal,
2034
Myoclonus
in hypoxic-ischemic encephalopathy,
571t
Myofascial pain disorders,
375
Myogenic factor 5 gene,
2112
Myomosphorylase deficiency,
e603-2
Myopathy
reversible infantile cytochrome C oxidase deficiency,
2066-2067
Myosin light chain (MLC),
1527
Myositis, enteroviruses in,
1092
Myotonia fluctuans,
2125t
Myotonia in myotonic muscular dystrophy,
2123-2124
Myotonia permanens,
2125t
Myotonic chondrodystrophy,
2125
Myringitis, bullous,
2199
Myxedematous syndrome,
1907
N
N-Acetylglutamate (NAG) synthetase deficiencies,
448f,
449-451
NADH cytochrome B5 reductase deficiency,
1673
Nafarelin for endometriosis,
690-691
Nafcillin,
e173-4t-e173-11t
for bacterial meningitis,
2093t
for cystic fibrosis lung infection,
1492t
for infective endocarditis,
1625t
for neonatal infection,
645t
for septic arthritis,
2400
for
Staphylococcus aureus,
907t
Nail(s)
effects of malnutrition on,
175t
juvenile dermatomyositis and,
847,
847f
Naloxone
in neonatal resuscitation,
576
for pediatric resuscitation and arrhythmias,
294t
Naphazoline hydrochloride for allergic conjunctivitis,
811t
Naprosyn for pain management,
364t
Naproxen
for juvenile idiopathic arthritis,
838t
for spondyloarthritides,
e150-2
Naproxen sodium for migraine,
2043
Naratriptan for migraine,
2044t
Narcolepsy-cataplexy syndrome,
e587-5
Narcosis as delivery room emergency,
575
Narrow complex tachycardia,
288-289
Nasal cannula oxygen for respiratory distress and failure,
319
Nasal continuous positive airway pressure (CPAP),
51
Nasal masses, midline congenital,
1431,
1431f
Nasal obstruction in common cold,
1435
Nasal septum, congenital defects of,
1430
Nasogastric tube feeding,
990
Nasojejunal tube feeding,
990
Nasolacrimal duct obstruction,
2165
Nasopharyngeal airway,
319
Nasopharynx,
Neisseria meningitidis in,
929-930
Nasotracheal aspiration,
e366-3
National Accreditation for the Education of Young Children (NAEYC),
e15-1
National Cancer Institute cancer trials,
1732
National Cholesterol Education Program (NCEP),
479-480
National Cooperative Group Program, cancer mortality rate reduction due to,
e488-1f
National Hansen’s Disease Program,
e208-3
National Immunization Days (NIDs),
1087
National Institutes of Health (NIH)
on anaphylaxis diagnosis,
817,
817t
National organizations involved in quality improvement,
e2-8t
National Vaccine Injury Compensation Program (NVICP),
886
Native Americans
disease beliefs or practices of,
e4-2t
as special risk population,
6-7
Natriuretic peptide
brain, in pulmonary edema,
1469
Natural disaster, drowning during,
343
Natural killer (NK) cells,
722
abnormalities of
inheritance in abnormalities of,
e117-6
interaction with other immune cells,
e117-5
in neonatal immunity,
632
Navicular stress fracture,
2418
N-carbamyl-β-amino aciduria,
e83-8
Nebulizer
for anaphylaxis drug delivery,
818t
Necrolytic migratory erythema (NME),
e637-6
Necrotizing external otitis,
2197
Necrotizing pneumonia,
905
Nedocromil sodium
for allergic conjunctivitis,
811t
Needle exposure, infections via,
e168-1
Needle length for vaccine,
886
Neisseria
Moraxella catarrhalis versus,
e188-2
predisposition to infection due to immunodeficiency,
716t
Neisseria gonorrhoeae,
935-940
clinical manifestations of,
937
pathogenesis and pathology of,
936-937
prophylaxis following rape,
704,
704t
Neisseria meningitidis,
929-935
differential diagnosis of,
932
in septic arthritis,
2398
Neonatal behavioral syndrome, due to selective serotonin reuptake inhibitors,
625,
625f
Neonatal Intensive Care Unit Neurobehavioral Scale (NNNS),
624,
624t
Neonatal iron storage disease (NISD),
1383,
1393
Neonatal seizure syndrome,
2035
Neonatal sleep myoclonus,
e587-5
Nephritic factor (NeF),
755-756
in membranoproliferative glomerulonephritis,
1787
Nephritic syndrome, acute,
1779-1780
acute poststreptoccocal glomerulonephritis as,
1783-1785
Nephritis
Henoch-Schönlein purpura,
1789
Nephrogenic syndrome of inappropriate antidiuresis,
216,
1884
Nephrology
See also Urologic disorders
cortical necrosis in,
1818
glomerulonephritis in
associated with systemic lupus erythematosus,
1788-1789
hematuria in
anatomic abnormalities associated with,
1796-1799
due to congenital anomalies,
1796
due to idiopathic hypercalciuria,
1795
isolated glomerular disease with recurrent gross,
1781-1783
lower urinary tract causes of,
1799
in thin basement membrane disease,
1783
due to vascular abnormalities,
1794
due to vigorous exercise,
1799
Henoch-Schönlein purpura nephritis in,
1789
polycystic kidney disease in
tubular disorders in
Gitelman syndrome as,
1814
nephrogenic diabetes insipidus as,
1812
Nephroma, mesoblastic,
1760
Nerve ablation and destruction,
373
Netilmicin,
e173-3
for cystic fibrosis lung infection,
1492t
for neonatal infection,
645t
Nettleship-Falls ocular albinism,
425
Neuraminidase inhibitors for influenza,
1123
Neuraminidase protein in influenza virus,
1122
Neuritis
sciatic, acute traumatic,
1085t
Neuroacademic problems,
e29-7
Neuroblastoma,
1753-1757
incidence and survival rates for,
1726t
juvenile idiopathic arthritis
versus,
835
Neurocristopathy syndrome,
1754t
Neurocutaneous syndromes,
2046-2053
linear nevus syndrome as,
2052
von Hippel-Lindau disease as,
2052
Neurodegeneration, pantothenate kinase-associated,
2057t,
2060
Neurodegenerative disorders,
2069-2076,
2070t
neuronal ceroid lipofuscinoses as,
2073,
2073t
Pelizaeus-Merzbacher disease as,
2074
subacute sclerosing panencephalitis as,
2075-2076
Neurodermatitis of external ear canal,
2199
Neurodevelopmental dysfunction,
e29-1-e29-9
assessment and diagnosis of,
e29-7
executive functioning,
e29-4
neuroacademic problems,
e29-7
spelling and writing impairments,
e29-6
terminology and epidemiology of,
e29-1
Neurodevelopmental function,
108
Neurodevelopmental variation,
108
Neuroferritinopathy,
2057t
Neuroleptic malignant syndrome (NMS),
65,
2059
Neurologic deficit
in sickle cell disease,
1667
Neurologic disorders,
565-574
central nervous system infections as,
2086-2098
congenital anomalies of central nervous system as,
1998-2013
failure to thrive in,
148t
manifesting as respiratory distress,
316
in mucopolysaccharidoses,
515t
neurocutaneous,
2046-2053
linear nevus syndrome as,
2052
von Hippel-Lindau disease as,
2052
psychopharmacology and,
65
Neurologic emergency(ies),
e63-1-e63-3
abusive head trauma as,
301
hypoxic-ischemic insult and encephalopathy as,
301-303
intracerebral hemorrhage as,
303-304
status epilepticus as,
303
Neurologic examination
general examination in,
e584-9
Neurologic manifestations and complications
of acute renal failure,
1821
after cardiopulmonary bypass,
1604
due to cat-scratch disease,
985
of congenital disorders of glycosylation,
e81-7t
of Epstein-Barr virus infection,
1114
due to immunosuppression therapy,
e437-3
of lysosomal storage disorders,
485t
of Neonatal Intensive Care Unit Neurobehavioral Scale,
624t
of
Shigella infection,
960
systemic inflammatory response syndrome and,
309t
of systemic lupus erythematosus,
843t
Neurologic system
overweight and obesity and,
183,
183f
prenatal development of,
e6-7f
shock-related dysfunction of,
307t
Neuroma, plexiform, of eyelid,
2165
Neuroma syndrome, mucosal,
1916
Neuromotor function, language disorders due to impairment of,
119
Neuromuscular blocking agents
analgesia and sedation with,
e70-3
Neuromuscular disorders
developmental,
2112-2119
benign congenital hypotonia as,
2119
brain malformations and,
2118
central core, minicore, and multicore myopathies as,
2117-2118
congenital muscle fiber-type disproportion as,
2115
muscular dysgenesis (proteus syndrome myopathy) as,
2119
effects of nerve agents on,
e704-3
hereditary motor-sensory neuropathies as,
2138-2140
myocardial disease with,
1629t
of neuromuscular transmission and motor neurons,
2132-2138
poliovirus infection
versus,
1085t
respiratory distress due to,
315t
Neuromuscular symptoms, terrorism and,
e704-8
Neuromuscular transmission disorders,
2132-2138
Neuromyopathy of severe illness,
1524
Neuronal apoptosis inhibitory gene,
2137
Neuronal ceroid lipofuscinoses (NCLs),
2073,
2073t
Neuronal heterotopias,
2004
Neuronal injury in seizures,
2025
Neuronal plasticity,
e6-1
Neuropathy
of Chédiak-Higashi syndrome,
744
poliovirus infection
versus,
1085t
Neuropsychiatric disorders associated with
Streptococcus pyogenes,
81,
919
movement disorders associated with,
76
Neurotoxicity, anesthesia-induced,
360,
e70-17
Neurotoxic shellfish poisoning,
e703-4
Neurotoxin, botulism,
987
Neurotransmitter precursors for BH
4 deficiency,
421
Neurotransmitters
sudden infant death syndrome and,
1422
Neutral lipid storage disease,
2268t
Neutral Protamine Hagedorn (NPH) insulin,
1976,
1977f
Neutropenia,
746-750
in bone marrow disorders,
749
in granule sorting disorders,
751
in immune function disorders,
751-752
in metabolic disorders,
751
in 3-methylglutaconic aciduria,
433
in Shwachman-Diamond syndrome,
750-751
in type I glycogen storage disease,
493
Neutrophil count
in acutely ill child evaluation,
277
in fever of unknown origin,
901
Nevoid telangiectasia,
2230
Newborn
antibiotic therapy for,
e173-1
breast abnormalities in,
e545-1
breathing patterns in,
580
complement system reductions in,
756
delivery room emergencies of,
575-579
abdominal wall defects as,
578
failure to initiate or sustain respiration as,
575
meconium staining as,
577
respiratory distress and failure as,
575
diabetes mellitus of,
1995
digestive system disorders of,
600-612
jaundice and hyperbilirubinemia as,
603-608
meconium ileus in cystic fibrosis as,
601,
601f
meconium peritonitis as,
601
dysmorphology in,
e102-6f
mechanisms, terminology, and definitions of,
e102-1t
fever without a focus in,
896t
fever without localizing signs in,
896-897
genitourinary system of,
e98-1
gynecological examination of,
e542-1
hyperthyroidism in,
1913f
infections in,
629-648
complications and prognosis for,
646,
647t
genital mycoplasma as,
1033
Haemophilus influenzae in,
943
systemic inflammatory response syndrome due to,
637-639
intellectual disability in,
125t
metabolic disturbances in,
622-626
metabolic bone disease as,
623
due to selective serotonin reuptake inhibitors,
625,
625f
neurologic disorders of,
565-574
due to inflammation, infection, and medications,
568-569,
568f
of spine and spinal cord,
573
parent-infant attachment/bonding and,
538-540
peripartum and postpartum factors in,
e7-1,
e7-2t
perception and effects of pain on,
373-375
physical examination of,
532-536
growth and behavior,
e7-1
red blood cell life span in,
e440-6
respiratory tract disorders of,
579-599,
579f
foramen of Morgagni hernia as,
597,
597f
foreign material aspiration as,
590,
591f
paraesophageal hernia as,
597
persistent pulmonary hypertension of the newborn as,
592-594,
592f
pulmonary hemorrhage as,
599
respiratory distress syndrome as,
581-590
transient tachypnea as,
590
routine delivery room and initial care of,
536-538
antiseptic skin and cord care in,
537
maintenance of body heat in,
536-537
transition of to pulmonary respiration in,
579-580
Newborn Behavior Assessment Scale (NBAS),
e7-3
New-onset refractory status epilepticus (NORSE),
2038
Nicotinamide-adenine dinucleotide phosphate (NADPH),
745
Nicotinamide for Hartnup syndrome,
430
Nicotinic acid for hyperlipidemia,
481t,
482
Niemann-Pick disease (NPD),
484t,
488
Nifedipine
for hypertensive emergencies,
1646t
for pulmonary hypertension,
1602t
Night blindness,
2154
due to vitamin A deficiency,
189
Nipple pain due to breast-feeding,
160
Nissen fundoplication,
527
Nitisinone for tyrosinemia,
422
Nitric oxide (NO)
adolescent huffing of,
681t
inhaled
for congenital diaphragmatic hernia,
595
for persistent pulmonary hypertension of the newborn,
593
for respiratory distress and failure,
319,
586
in rectal dialysate,
1344t
Nitrites
adolescent abuse of,
675t
Nitroglycerin
for cardiogenic shock,
313t
Nitroprusside
for cardiogenic shock,
313t
for hypertensive emergencies,
1646t
Nizatidine for
Helicobacter pylori gastritis,
1293t
N,N-diethyl-
m-toluamide (DEET)
for malaria prevention,
1207
for tularemia prevention,
980
Nodes, with cat-scratch disease,
984
Nodular lymphoid hyperplasia (NLH),
e337-3
Nodule(s)
in autoimmune thyroiditis,
1905
subcutaneous
in acute myeloid leukemia,
1737
in acute rheumatic fever,
922
of thyroid carcinoma,
1914
Nonalcoholic fatty liver disease (NAFLD),
184t
Nonallelic homologous recombination,
e74-5
Nonbicarbonate buffers,
e52-13
Noncomitant strabismus,
2159
Nondiscrimination, chronic illness and,
e39-3
Nondisjunction, chromosomal,
400
Nonedematous malnutrition,
175
Nonfatal injuries,
19,
19f
Non-germ cell gonadal tumors,
1770
Nongonococcal urethritis (NGU)
Trichomonas vaginalis in,
1186
Non-heart-beating donor (NHBD),
e3-3
Noninflammatory diarrhea,
1330
Noninvoluting congenital hemangioma (NICH),
2229
Nonketotic hyperglycinemia (NKH),
439-440
Nonketotic hyperosmolar coma,
1981
Nonmenstrual toxic shock syndrome and,
908
Non-nucleoside reverse transcriptase inhibitors (NNRTIs),
1162t
Nonnutritive sweeteners,
1982
Non-polyanaline repeat expansion mutation (NPARM),
1520-1521
Non-rapid eye movement (NREM), respiratory regulation in,
e365-14
Non-REM partial arousal disorders,
e587-5
Nonsteroidal antiinflammatory drugs (NSAIDs)
gastric ulcer due to,
1293
for juvenile idiopathic arthritis,
837,
838t
pseudoporphyria due to,
e148-3
topical, for skin disorders,
2217
Nontherapeutic research,
e3-5
Norepinephrine,
e568-1-e568-8,
e568-8f
for cardiac output maintenance and post-resuscitation stabilization,
294t
genetic disorders of,
445t
in pheochromocytoma,
1942
Norfloxacin for traveler’s diarrhea,
e168-5
Nortriptyline
for attention deficit/hyperactivity disorder,
111t
for pain management,
364t
Nose
fracture of, as delivery room emergency,
579
saddle deformity
in Wegener’s granulomatosis,
874,
875f
Nosocomial infection
fever of unknown origin in,
899t
respiratory syncytial virus,
1127
Nosocomial pneumonia,
Pseudomonas aeruginosa in,
976
Notching of inferior border of ribs,
1568
Nuclear factor
KB essential modulator (NEMO) mutations,
726
Nuclear medicine imaging
in aspiration syndromes,
1472t
in congenital hypothyroidism,
1900
in fever of unknown origin,
902
in neonatal cholestasis,
1385
in orthopedic problems,
2334
in pulmonary embolism,
1502
radiation exposure from,
2448
in septic arthritis,
2400
Nucleic acid amplification,
e164-4
Nucleic acid amplification testing (NAAT)
in gonococcal disease,
938
in
Mycobacterium tuberculosis,
996
in sexually transmitted disease,
709
Nucleoside/nucleotide analogs,
1399
Nucleoside/nucleotide reverse transcriptase inhibitors (NRTIs),
1167,
1168t-1171t
Numerical Rating Scale (NRS) for pain assessment,
361
Nutrition
See also Diet See also Malnutrition
acute intermittent porphyrias and,
e85-5
in acute renal failure,
1821
assessment of before renal transplantation,
e530-2
in chronic kidney disease,
1824
in eating disorders treatment,
94-95
effects of vomiting on,
1243t
ethics of withholding,
e3-2
feedings in
of school-age children and adolescents,
166-167
of toddlers and preschool-age children,
165
issues associated with
complementary and alternative medicine,
169
food assistance programs,
170
in gastroesophageal reflux disease,
1269
nutritional programming,
169
preventive nutrition counseling,
169-170
using food as reward,
167
overweight and obesity and,
179-188
endocrine and neural physiology of,
183
environmental factors in,
182
parenteral
cholestasis associated with,
e352-2
for premature and low birthweight infants,
559-560
for short bowel syndrome,
1316
in
Shigella treatment,
961
vitamin A deficiencies and excess in,
188-191
vitamin B complex deficiency and excess in,
191-198
Nystagmus retractorius,
2161
O
Oasthouse urine disease,
1319
Obesity,
179-188
endocrine and neural physiology of,
183
environmental factors in,
182
pulmonary manifestations of,
e413-1t
sleep-disordered breathing and,
49
Object, transitional,
31-32
Observation
in acutely ill child evaluation,
276
in brain death diagnosis,
e63-3
Obsessive-compulsive disorder (OCD),
80-81,
81t
group A streptococci infection and,
919
trichotillomania as,
2290
Obstruction
airway
critical high airway obstruction syndrome (CHAOS),
577,
578f
respiratory distress due to,
315t
in respiratory syncytial virus infection,
1127-1128
due to tonsil and adenoid pathology,
1443,
1445
congenital nasolacrimal duct,
2165
nasal in common cold,
1435
Obstructive congenital heart disease,
1561-1571
Obstructive disorders of esophagus,
1263-1264
Obstructive jaundice in cystic fibrosis,
1496
Obstructive shock,
285,
305,
307t
clinical manifestations of,
308
hemodynamic variables in,
311t
Obstructive sleep apnea,
403t
Obstructive uropathy, nephrotoxins in,
1817t
Occipital plagiocephaly,
2012
Occult blood, fecal,
1344t
Occupants in motor vehicle accident,
21-22
Occupational therapy
for juvenile dermatomyositis,
849
for respiratory insufficiency,
1525
Ochronosis in alcaptonuria,
423
Octopia lentis, in Marfan syndrome,
2441-2442
Octreotide
for chemotherapy-associated vomiting,
1244t
Ocular motor apraxia, congenital,
2161
Oculocephalic reflex, brain death and,
e63-2t
Oculocutaneous tyrosinemia,
422-423
Oculoglandular tularemia,
979
Oculomotor apraxia type Cogan,
1816
Oculomotor nerve
neurologic examination of,
e584-4
seizures and abnormalities of,
e587-4
Oculosympathetic paresis,
2155
Oculovestibular reflex, brain death and,
e63-2t
Odor
inborn errors of amino acid metabolism associated with,
418t
Office
isolation techniques for,
e166-1
microbiologic testing in,
e164-3
OKT3 in renal transplantation,
e530-3
Olanzapine for psychosis and agitation,
64t
Olfactory nerve, neurologic examination of,
e584-3
Oligohydramnios
high-risk infant due to,
552
Oliguria, fluid therapy adjustments and,
245,
245t
Olopatadine
for allergic conjunctivitis,
811t
Omalizumab
for allergic disease,
772
for atopic dermatitis,
805
Omphalomesenteric duct, remnants of,
1281-1282
Ondansetron
for chemotherapy-associated vomiting,
1244t
Ondansetron for vomiting,
1244t
Oocyst in toxoplasmosis,
1208
Oophoritis, due to mumps,
1080
Operating otoscope head,
2202
Operations Management,
e2-5
Ophthalmia neonatorum,
2166
Ophthalmitis, gonococcal,
937
Ophthalmologic examination,
2148-2150,
2149t
fever of unknown origin and,
901
in juvenile idiopathic arthritis,
833t
Ophthalmopathy, thyroid-related,
2182
Ophthalmoplegia
internuclear in neurologic examination,
e584-4
Opioids
for neuropathic pain,
368t
Opportunistic infections (OIs)
chronic diarrhea due to,
1340
Pseudomonas aeruginosa,
975
Opsoclonus myoclonus syndrome,
e587-5
neuroblastoma associated with,
1754t
Optic disc
disorders of
morning glory anomaly as,
e623-1
neurologic examination of,
e584-2
Optic nerve
multiple sclerosis effects on,
2077t
myelination of fibers of,
2181
traumatic injury to,
2185
Optic nerve aplasia,
2181
Optic nerve hypoplasia,
e623-1
Oral allergy syndrome,
822
Oral cavity
disorders of
associated with other conditions,
1251,
1251t
of salivary glands and jaw,
e308-1
effects of malnutrition on,
175t
newborn assessment of,
534
Oral hairy leukoplakia,
2299
Oral hygiene for dental caries prevention,
1256
Orbit
complications of due to sinusitis,
1438
penetrating wounds of,
2186
Orbital inflammation,
2182
Orbital pseudotumor,
2182
Organ dysfunction in shock,
305,
307t
Organic anion transporting polypeptides (OATPs),
e56-10
Organic cation transporters (OCTs),
e56-10
Organizational stage of empyema,
1507
Organization skills,
e29-4
Organophosphates poisoning,
266-267
Orificial tuberculosis,
2307
Orlistat
for weight loss in adults,
187t
Ornithine transcarbamylase (OTC) deficiency,
448f,
451
Oropharyngeal airway for respiratory distress and failure,
319
Oropharyngeal infections
Francisella tularensis in,
979
Orthographic problems,
e29-6
Orthopedic management of arthrogryposis,
e674-3
Orthopedic problems
disorders of in mucopolysaccharidoses,
515t
of hip,
2355-2365
slipped capital femoral epiphysis as,
2363,
2364f
transient monoarticular synovitis as,
2360
in juvenile idiopathic arthritis,
838-839
of knee,
2351-2355
idiopathic adolescent anterior knee pain syndrome as,
2354
patellar subluxation and dislocation,
2355
of spine,
2365-2377,
2365t
intervertebral disk herniation and slipped vertebral apophysis as,
2377
syndromes and genetic disorders,
2371
in systemic lupus erythematosus,
843t
Orthopedic prostheses, infection associated with,
e172-3
Orthostatic proteinuria,
1800
Orthotopic liver transplantation (OLT),
1414
Osmolality,
e52-2-e52-3
in diabetes insipidus,
1882
of intravenous solutions,
217,
243
in nephrogenic diabetes insipidus,
1812
Osmolarity of oral rehydration solutions,
1335t
Osmotic equilibrium,
e52-2
Ossifying fibroma of jaw,
e308-1
Osteogenesis imperfecta (OI),
2437-2440
dentinogenesis imperfecta with,
1250
laboratory findings in,
2439
middle ear and inner ear involvement in,
e633-1
Osteoma of ear canal,
2199
Osteomyelitis
differential diagnosis of,
2397
Pseudomonas aeruginosa,
976t
Osteonecrosis in slipped capital femoral epiphysis,
2365
Osteopathia striata,
2222
Osteoporosis-pseudoglioma,
2447
Otitic hydrocephalus,
2212
Otitis media (OM),
2199-2213
in cleft lip and palate,
1253
clinical manifestations of,
2202
as complication of common cold,
1436
developmental sequelae of,
2213
external otitis
versus,
2197
Haemophilus influenzae in,
943
Moraxella catarrhalis in,
e188-1
nontuberculous mycobacterial,
1013
in parainfluenza viruses,
1125t
with Turner syndrome,
1953
Otoacoustic emissions (OAE) testing,
2192,
2195
Otomastoiditis, nontuberculous mycobacterial,
1013
Outcome measures in emergency medical services for children,
278,
e61-10
Outpatient setting, isolation techniques for,
e166-1 See also Office
Ovary(ies)
autoimmune failure of,
1956
Overdose syndrome, opiate,
685
Overlapping 5th toe,
2342
Over-the-counter (OTC) preparations
Overweight,
36t,
179-188
endocrine and neural physiology of,
183
environmental factors in,
182
sleep-disordered breathing and,
49
systemic hypertension and,
1641
type 1 diabetes mellitus and,
1982
Ovotesticular disorders of sex development (DSD),
1968
Oxalate-containing plants toxicity,
269t
Oxandrolone for Turner syndrome,
1954
Oxcarbazepine
adverse effects of,
2031t
Oxidative phosphorylation (OXPHOS), impaired,
1405-1406
Oxides of nitrogen (NO
x),
e700-1
Oxybutynin for nocturnal incontinence,
1852
Oxycodone
equianalgesic doses and half-life of,
367t
for pain management,
365t
Oxycontin for pain management in palliative care,
155t-156t
Oxygen
hyperbaric for carbon monoxide poisoning,
270
partial pressure of,
e365-3f
divided into fraction of inspired oxygen,
319
in fetal circulation,
1529
in respiratory alkalosis,
240
in respiratory failure,
316
in transitional circulation,
e415-1
Oxygen administration
in neonatal resuscitation,
576
in premature infant,
559
possible adverse reactions to,
563t
for respiratory distress and failure,
319,
584
Oxygenation assessment in respiratory distress and failure,
318-319
Oxygen-hemoglobin dissociation curve,
e365-3f
Oxyhemoglobin (So
2),
1419
Oxymetazoline for allergic rhinitis,
780t
Oxysterol 7α-hydroxylase deficiency,
1384
P
Pachyonychia congenita,
2273
Pacific Islander population, death rates for,
3t-4t
Pacifiers
sudden infant death syndrome and,
1425
Pain
abdominal,
1247-1248,
1247t-1248t
in acute intermittent porphyrias,
e85-6
in acutely ill child,
276
in
Campylobacter infection,
969
exclusion from day care due to,
e15-2t
in hyperparathyroidism,
1921
nondigestive causes of,
1241t
of peptic ulcer disease,
1292
chest
differential diagnosis of,
1530t
as manifestation of extrapulmonary disease,
1526,
e413-1t
due to chronic illness,
e39-2
congenital insensitivity to,
2143
muscular, in neuromuscular disorders,
2109
not result of identifiable or diagnosable conditions,
375
perception and effects of on newborns and infants,
373-375
due to sports injury,
2408
Pain disorder
diagnostic criteria for,
68t,
69
Pain management,
360-375
for advanced disease,
374
invasive interventions for,
371-373
pharmacologic,
362-370,
368f
acetaminophen, aspirin, and nonsteroidal antiinflammatory drugs for,
363-364,
364t
antipsychotics and major sedatives for,
370
pharmacokinetics and pharmacodynamics of analgesics in,
362-363
serotonin and selective serotonin reuptake inhibitors for,
369
Pain receptors in respiration regulation,
1421
Pain syndrome(s)
myofascial pain disorders and fibromyalgia,
375
Palliative care,
149-159,
150f
communication, advanced care planning, and anticipatory guidance in,
151-159
Pallister-Hall syndrome (PHS),
e102-3-e102-4
adrenal insufficiency with,
1925t
congenital heart disease with,
1531t
Pallister-Killian syndrome,
412
Pallor
in iron deficiency-anemia,
1656
Palmar erythema, as manifestation of liver disease,
1376
Palmaris longus muscle aplasia,
2118
Palpation
abdominal
in acutely ill child evaluation,
276-277
of skull in neurologic examination,
e584-2
Pancreas
disorders of
associated with pancreatic insufficiency,
1369-1370
pancreatic function tests in,
e340-1
Pancreatic agenesis,
1368
Pancreatic function tests,
e340-1
Pancreatic panniculitis,
2284
Panton-Valentine leukocidin (PVL),
904
Pantothenate kinase-associated neurodegeneration,
2057t,
2060
Paper wasp, allergic responses to,
807f
Papillon-Lefèvre syndrome,
2273
Papular acrodermatitis of childhood,
2266,
2266f
Papular-purpuric “gloves and socks” syndrome (PPGSS),
1096-1097,
1096f
Paracentric chromosomal inversion,
405-406
Paradoxical pupil reaction,
2156
Paraldehyde for status epilepticus,
2039t
Paralysis
pharmacologic in mechanical ventilation,
328
Paramedics (EMT-P),
e61-3
Parasitic infections
fever of unknown origin in,
900t
helminthic
Gnathostoma spinigerum,
1227
in immigrant children,
133
laboratory diagnosis of,
e164-4
maternal
fetal and neonatal effects of,
e89-3t
predisposition to due to immunodeficiency,
716t
traveler’s diarrhea due to,
1338t
Parathyroid hormone (PTH)
disorders of
pseudohypoparathyroidism (Albright hereditary osteodystrophy),
1919-1920
Parathyroid hormone-related peptides (PTHrP),
e564-2
Parenchymal lung disease
emergency airway management in,
284
Parent(s)
genetic counseling and,
378
presence during induction of anesthesia,
e70-8
psychologic changes in during pregnancy,
e6-8
role in maternal-infant attachment,
e7-1,
e7-1t
Parental permission,
e3-1
Parenteral drug administration,
e57-11
Parenteral nutrition,
1316
Parent-infant bonding/attachment,
538-540
Parents’ Evaluation of Developmental Status (PEDs),
41t-43t
Parkinsonism, infantile,
445
Paronychia, candidal,
1055
Paroxetine for premenstrual dysphoric disorder,
692t
Paroxysmal cold hemoglobinuria,
1683
Paroxysmal depolarization shift (PDS),
2025
Paroxysmal dyskinesias,
e587-3
Paroxysmal extreme pain disorder,
e587-3
Paroxysmal hypercyanotic attacks in tetralogy of Fallot,
1574
Paroxysmal kinesigenic choreoathetosis (PKC),
2057t
Paroxysmal stage of pertussis,
945
Paroxysmal torticollis of infancy,
2379
Parry Romberg syndrome,
851t
Partial agonists, receptor binding by,
e57-8
Partial hospital program (PHP) for eating disorders,
96
Partial liquid ventilation (PLV),
596
Partial pressure of carbon dioxide (PCO
2),
e365-3f
in respiratory failure,
316
Partial pressure of oxygen in inspired gas (Pio
2),
e365-7
Partial pressure of oxygen (Po
2),
e365-3f
divided into fraction of inspired oxygen,
319
in fetal circulation,
1529
in respiratory alkalosis,
240
in respiratory failure,
316
in transitional circulation,
e415-1
Partial rebreather mask,
319
Partial thromboplastin time,
1697
Passiflora alata for sedation,
271t
Passionflower for sedation,
271t
Passive immunity, immunization for,
881-883
Passive muscle tone,
2109
Pastes for skin disorders,
2216
Past medical history
in acutely ill child,
276
Patellar subluxation and dislocation,
2355,
2415
Patellar tendinosis,
2416
in basketball and volleyball,
e684-2
Patellofemoral disorders,
2354
Patellofemoral stress syndrome (PFSS),
2415-2416
Patent ductus arteriosus (PDA),
1559-1561,
1560f
respiratory distress syndrome and,
587
Patent foramen ovale (PFO),
1551
Pathogen-associated molecular patterns (PAMPs),
855
Pathogenicity islands, group B streptococci,
926
Patient, discussion of cancer treatment with,
e488-3
Patient and family education
for child abuse prevention,
142
in diabetes mellitus management,
1979
in functional abdominal pain,
1348
in psychosomatic illness,
70
Patient-centered care,
e2-1
Patient-controlled analgesia (PCA)
Patient positioning
for female genital examination,
1425
in gastroesophageal reflux disease,
1268
sudden infant death syndrome and,
1425
Pattern recognition receptors (PRRs),
855
Pausinystalia yohimbe, potential toxicity of,
272t-273t
Peak expiratory flow (PEF)
Peak inspiratory pressure (PIP)
in mechanical ventilation,
328
Pediatric autoimmune neuropsychiatric disorders associated with
Streptococcus pyogenes (PANDAS),
81,
919
movement disorders associated with,
76
Pediatric gait, arms, legs, spine screen (pGALS),
e664-2
Pediatric Rhinoconjunctivitis Quality of Life Questionnaire (PRQLQ),
776
Pediatric Risk of Mortality (PRISM) scoring system,
e2-3
Pediatrics,
1-13
growth of specialization of,
12-13
health among postinfancy children and,
2-4
health care costs and,
11
information explosion of 21st century and,
11-12
organization of the profession,
12-13
patterns of health care in,
9
planning and implementing a system of care in,
9-11
scope and history of,
1-5
special risk populations in,
5-9
Pediatric transport medicine,
e61-7
Pediatric unstable bladder,
73
Pediculosis capitis,
2321
Pediculosis corporis,
2321
Pediculus humanus var.
corporis,
986
Peeling skin, familial,
2268t
Peeping undescended testis,
1859
Peers, adolescent development of relationships with,
650t,
652-654
Pegaspargase for cancer therapy,
e488-4t
Peg-shaped lateral teeth,
1250
Pegvisomant for growth hormone excess,
e554-4
Pelizaeus-Merzbacher disease (PMD),
2074
Pelodera strongyloides,
1220t
Pelvic inflammatory disease (PID),
708,
939,
1871
dysmenorrhea due to,
691t
Pelvis
fetal ultrasound of,
550t
musculoskeletal pain syndrome of,
877t
urinary tract obstruction of,
1839t
Pemirolast potassium,
811t
Pemphigus vulgaris (PV),
2247
Pena-Shokeir syndrome,
2138
Penetrating wounds of orbit,
2186
Penicillin,
e173-3
for group A streptococci infection,
918
for vulvovaginitis,
1868t
Penicillin G,
e173-4t-e173-11t
for bacterial meningitis,
2093t
for group A streptococci,
918
for group B streptococci,
927
for infective endocarditis,
1625t
for meningococcal disease,
933t
for neonatal infection,
645t
Penicillin G, benzathine,
645t
for acute rheumatic fever prophylaxis,
924t
for group A streptococci infection,
918
for neonatal infection,
645t
for sexually transmitted infections in adolescents,
712t
Penicillin G, procaine,
645t
for neonatal infection,
645t
Penicillin V,
e173-4t-e173-11t
for acute rheumatic fever prophylaxis,
924t
for group A streptococci infection,
918
for post-splenectomy prophylaxis,
e481-1
Penile curvature, lateral,
1857
Pentalogy of Cantrell,
1599
Pentobarbital
for traumatic brain injury,
300
Pentobarbital coma for status epilepticus,
2039t
Pentosuria, essential,
e81-5
Peppermint oil for functional abdominal pain,
1348t
Peptide absorption disorders,
1318
Percentile, statistical,
e6-6
Perceptual functioning,
e29-2-e29-3
elementary school success and,
37t
Percutaneous drug administration,
e57-11
Percutaneous umbilical blood sampling (PUBS),
543t,
544,
549
in erythroblastosis fetalis,
617
Perennial allergic conjunctivitis,
809-810
Perennial allergic rhinitis (PAR),
775
Performance Improvement (PI),
e2-3
Performance management,
e2-1t
Performance measure,
e2-1t
Perfusion, shock-related decrease of,
308t
Perfusion pressure, cerebral,
296,
297f
Perianal candidosis,
2314
Perianal pruritus in enterobiasis,
1222
Pericardial effusion, tuberculous,
1009
Pericardiocentesis for emergencies,
295-296
Pericarditis
in acute rheumatic fever,
922
in chronic kidney disease,
1823t
Haemophilus influenzae in,
942
Pericentric chromosomal inversion,
405-406
Perifollicular petechiae, due to vitamin C deficiency,
198-199,
199f
Perinatal infections,
543t,
547-548
congenital lymphocytic choriomeningitis,
548
Perineal pruritus in enterobiasis,
1222
Perinuclear antineutrophil cytoplasmic antibody (pANCA),
1295
Periodic breathing pattern in newborn,
580
Periodic fever, aphthous stomatitis, pharyngitis, and adenitis (PFAPA),
859-860
Periodicity Schedule,
14,
15f
Periodic limb movement disorder (PLMD),
52-53
Peripartum influences on maternal-infant attachment,
e7-1
Peripheral blood smear
in iron deficiency anemia,
1657f
Peripheral vascular resistance (PVR),
592,
592f
Peripheral vascular system disease
arteriovenous fistula as,
e438-1
Peritoneum disorders
epigastric hernia as,
1418
Peritonsillar cellulitis/abscess,
1440,
1442
Periungual candidal infection,
1055
Periventricular leukomalacia (PVL),
566-568
optic nerve hypoplasia with,
e623-1
Permanent neonatal diabetes mellitus (PNDM),
1995
Permission, parental,
e3-1
Permissive hypercapnia in mechanical ventilation,
585
Permissive hypoxemia in mechanical ventilation,
585
Peroral drug administration,
e57-11
Peroxisomal disorders,
462-467
genetic counseling in,
467
Persistent fetal vasculature,
2176
Persistent hyperinsulinemic hypoglycemia of infancy (PHHI),
522-523
Persistent müllerian duct syndrome,
1964-1965
Persistent pulmonary hypertension of the newborn (PPHN),
592-594,
592f,
1420
Persistent pupillary membrane,
2156
Persistent rhinitis (PR),
775
Personal flotation device (PDF),
24
Personal protective equipment (PPE),
e166-2t
Pertussis,
944-948
clinical manifestations of,
945
exclusion from day care due to,
e15-2t
Pervasive developmental disorders (PDD),
100,
101t-102t
language disorders of,
118
Pet therapy for pain management,
371
Pfaundler-Hurler disease,
512t
pH,
230t,
e52-13
in acid-base disorders,
230
esophageal
in aspiration syndromes,
1472t
in gastroesophageal reflux disease,
1267
of fetal scalp blood,
544
Phakomatosis pigmentovascularis,
2226
Phalangeal fracture,
2391
Pharmacobetabonomics,
e56-4
Pharmacogenetic testing in acute lymphocytic leukemia,
1736
Pharmacogenomics,
e56-1
development of pediatric,
e56-2
internet resources for,
e56-7t
Pharyngeal culture in gonococcal disease,
938
Phencyclidine (PCP) abuse,
676t,
683
Pheniramine maleate,
811t
Phenobarbital
adrenal insufficiency due to,
1927
adverse effects of,
2031t
for hypoxic-ischemic encephalopathy,
571
neonatal withdrawal from,
624
possible adverse reactions to in premature infant,
563t
for vomiting prophylaxis,
1244t
Phenotypes
correlation with genotype in genetic disease,
e74-4
Phentermine for weight loss in adults,
187t
Phenylephrine
for allergic rhinitis,
780t
Phenytoin
adrenal insufficiency due to,
1927
adverse effects of,
2031t
gingival overgrowth due to,
1257
for hypoxic-ischemic encephalopathy,
571
Philodendron toxicity,
269t
Phlebotomy for porphyria cutanea tarda,
e85-12
Phobic hallucinations, acute,
106-107
Phonologic processing,
e29-6
Phonophobia in migraine,
2041
Phosphate, renal tubular regulation of,
e522-1
Phosphate and tensin homolog (PTEN),
e554-2t
Phosphoenolpyruvate carboxykinase (PEPCK) deficiency,
504
Phosphofructokinase deficiency,
1677
Phosphoribosylpyrophosphate (PRPP) synthetase superactivity,
e83-5-e83-6
Phosphoserine aminotransferase deficiency,
442
Photoallergic reaction,
2255
Photoparoxysmal epilepsy,
2023
Photophobia in migraine,
2041
Photosensitivity,
2254-2259
in congenital erythropoietic porphyria,
e85-9
in erythropoietic protoporphyria,
e85-16
in systemic lupus erythematosus,
e637-4f
Phototherapy
for atopic dermatitis,
805
for hemolytic disease of newborn due to ABO blood group incompatibility,
619
PHOX2B gene
congenital central hypoventilation syndrome and,
1520-1521
ventilator dependence and,
1520
Phrenic nerve injury in newborn,
574
Physical activity
in eating disorders treatment,
94-95
energy requirements and,
e41-1t
overweight and obesity and,
182,
186
Physical development
adolescent
during late adolescence,
654
during middle adolescence,
653
assessment of
accurate measurements in,
e13-1
body proportions in,
e13-4
skeletal maturation in,
e13-4
structural growth in,
e13-4
during preschool years,
33-34
Physical education, congenital heart disease and,
1603
Physical examination
in attention deficit/hyperactivity disorder,
110
in communication disorder,
121
in failure to thrive,
149t
in fever of unknown origin,
901,
901t
in genetic metabolic disease,
416-417
in hemostatic disorders,
1696
in intellectual disability,
127t
Physical therapy
for juvenile dermatomyositis,
849
for respiratory insufficiency,
1525
Physiologic studies, sudden infant death syndrome and,
1428
Physiotherapy for Duchenne and Becker muscular dystrophy,
2122
Physostigmine as poisoning antidote,
256t-257t
Phytolacca americana, potential toxicity of,
272t-273t
Pigeon fancier or breeder lung,
1473
Pigmentation, McCune-Albright syndrome in abnormal,
1892,
1892f
Pilomyxoid astrocytoma,
1749
Pineal parenchymal tumor,
1752
Pinna
pits and sinus tracts anterior to,
2221
Piperacillin-tazobactam,
e173-4t-e173-11t
for cystic fibrosis lung infection,
1492t
for neonatal infection,
645t
Pseudomonas aeruginosa,
977
Piper methysticum for sedation,
271t
Pirbuterol for asthma,
796
Pituitary gland
puberty physiology and,
e555-1
Pituitary gland disorders
fetal and neonatal overgrowth as,
e554-5
hypothyroidism due to disease of,
1901
tumors of, adrenal insufficiency due to,
1926t
Pityriasis lichenoides chronica (PLC),
2260-2261
Pityriasis lichenoides et varioliformis acuta (PLEVA),
e163-1
Placenta
chemical pollutants crossing,
e700-3
vascular anastomoses in monochorionic twins,
554
Plain radiographs
in liver dysfunction,
1379
in neonatal necrotizing enterocolitis,
602
in septic arthritis,
2399
Plan-Do-Study-Act (PDSA) cycle,
e2-3f
Plantar response assessment in neurologic examination,
e584-7
Plaque, examination of,
2215
Plasma anion gap in metabolic acidosis,
233-234
Plasma complement control protein deficiency,
755
Plasma concentration of drug,
e57-10
Plasmalogen synthesis, isolated defects of,
464-465
Plasma membrane carnitine transport defect,
460-461
Plasma membrane in cardiac development,
1528
Plasma thromboplastin antecedent,
1696t
Plasma volume, hyponatremia due to decreased,
1885
Plasminogen, reference values for,
1698t
Plasminogen activator inhibitor, reference values for,
1698t
Plasminogen activator inhibitor deficiency,
1704
Platelet aggregation,
1698
Platelet count
in hemolytic-uremic syndrome,
1793
in Rocky Mountain spotted fever,
1042
Platelet-derived growth factor receptor α (PDGFRα),
e488-2t
Platelet-derived growth factor receptor β (PDGFRβ),
e488-2t
Platelet function analyzer,
1697
Play
in autistic disorder,
100
during preschool years,
34-35
Pleocytosis in enteroviral meningitis,
1091
Pleomorphic rhabdomyosarcoma,
1760
Plesiomonas shigelloides,
e196-1-e196-3
in infectious diarrhea,
1337t
inflammatory bowel disease
versus,
1298t
in traveler’s diarrhea,
1338t
Pleural fluid examination
Pleurodynia, due to enterovirus,
1090
Plexiform neuroma of eyelid,
2165
Pneumatic otoscope head,
2202
Pneumococcal conjugate vaccine (13 valent) (PCV 13),
884t,
889,
914t
Pneumonia,
1474-1479
aspiration
due to hydrocarbon toxicity,
267
Blastomyces dermatitidis,
1064
bronchiolitis obliterans organizing,
e386-1
Chlamydia trachomatis,
1037
differential diagnosis of,
1477t
Francisella tularensis,
979
Haemophilus influenzae,
942
interstitial
in lysinuric protein intolerance,
455
Mycoplasma pneumoniae,
1030
in parainfluenza viruses,
1125t
Pseudomonas aeruginosa,
976t
Streptococcus pneumoniae,
912f
ventilator-associated,
329
Podofilox
for human papillomavirus,
1140
Poison hemlock toxicity,
269t
Poisoning,
250-270
cardiac arrest due to,
289t
cardiovascular medications,
261-263
cholinesterase-inhibiting insecticides,
266-267
common nontoxic and minimally toxic products and,
251t
ibuprofen and other nonsteroidal antiinflammatory drugs,
260-261
lead,
2448-2453
δ-aminolevulinic acid dehydratase deficiency due to,
e85-4
major modes of presentation, drugs associated with,
255t
recognizable syndromes of,
253t
respiratory distress due to,
316
respiratory signs and symptoms of,
e413-1t
salt
plasma osmolality in,
e52-3
small dose medications,
251t
Policy(ies)
for emergency departments,
e61-4t
Policy of pay per performance (P4P),
e2-2
Poliovirus receptor,
1081
Pollen-food syndrome,
822
Pollutants
wheezing and bronchitis due to,
1460
Polyanaline repeat expansion mutation (PARM),
1520-1521
Polyarthritis
migratory, in acute rheumatic fever,
921-922
Polycystic kidney disease
autosomal dominant,
e357-2
congenital heart disease with,
1531t
Polycystic liver disease,
e357-2
Polycythemia rubra vera,
e460-1
Polydactyly syndromes, short-rib,
2434
Polydipsia
differential diagnosis of,
1882t
primary, hyponatremia due to,
1885
Polyendocrinopathy (APS),
1925t
Polyethylene glycol
for constipation maintenance therapy,
74t
for fecal disimpaction,
74t
Polygenic hypercholesterolemia,
473t,
475
Polyglucosan body disease,
497
Polyhydramnios
esophageal functioning and,
1261
Polymerase chain reaction (PCR),
376,
e164-4-e164-5
in Duchenne and Becker muscular dystrophy,
2120
in enterovirus infection,
1093
in parainfluenza viruses,
1125t
in respiratory syncytial virus infection,
1128
Polymorphonuclear leukocytes,
2220
Polymorphous light eruption,
2257
Polymyositis-scleroderma antibody,
e147-3t
Polyneuropathy
critical illness, poliovirus infection
versus,
1085t
Polyomavirus nephropathy (PVN),
e530-6
Polyostotic fibrous dysplasia,
1892
Polyp(s)
cervical, abnormal uterine bleeding due to,
689t-690t
endometrial, abnormal uterine bleeding due to,
689t-690t
juvenile polyposis syndrome,
e337-1
Polysomnogram (PSG),
50-51
Polysyllabic jargoning,
31
Polyunsaturated fatty acids (PUFAs),
e41-15
Polyuria
differential diagnosis of,
1882t
fluid therapy adjustments and,
245,
245t
Ponseti method for clubfoot treatment,
2337
Pontocerebellar hypoplasia,
2007
Population stratification,
e77-3
Porphobilinogen deaminase (PBGD) deficiency,
e85-4-e85-5
Position 57 in DQB1, type 1 diabetes mellitus and,
1970-1971
Positioning
for female genital examination,
1425
in gastroesophageal reflux disease,
1268
sudden infant death syndrome and,
1425
Positive end-expiratory pressure (PEEP),
327,
e365-2
expiratory phase maneuvers in,
326
for pulmonary edema,
1469
Positive pressure respiratory support for respiratory distress and failure,
320
Positive pressure ventilation
Positron emission tomography (PET),
e584-11
Postcoarctectomy syndrome,
1569
Postconcussive syndrome,
301
Postenteritis syndrome,
1340
Posterior cruciate ligament injuries,
2414
Posterior fossa tumors,
1748t
Posterior laryngeal cleft (PLC),
1452
Posterior lenticonus,
2172
Posterior sagittal anorectoplasty (PSARP),
1358
Posteromedial tibial bowing,
2351
Postexposure prophylaxis, hepatitis B,
1400
Posthemorrhage hydrocephalus (PHH),
567-568
Postinfection diarrhea,
1313
Post-kala-azar dermal leishmaniasis (PKDL),
1189
Postneonatal mortality,
e87-3
Postoperative nausea and vomiting (PONV),
e70-11
Postpartum thyroiditis,
1904t
Postpericardiotomy syndrome,
1604
Postrenal acute renal failure,
1819
Post-streptococcal arthritis,
840
Post-transplantation lymphoproliferative disorder (PTLD),
e171-2
Post-traumatic stress disorder (PTSD),
81-82,
82t
associated with war,
e36-6
Postural proteinuria,
1800
Posture in hypoxic-ischemic encephalopathy,
570t-571t
Potassium,
219-224,
e41-17
in acute renal failure,
1820
measurement of in intravenous rehydration,
247
in oral rehydration solutions,
1335t
periodic paralysis related to,
2130
renal tubular regulation of,
e522-1
urinary wasting of, hypokalemia in,
223
Potassium-aggravated myotonia,
2125t
Potassium channel autoantibodies, syndrome of,
e587-4
Potassium channel genes, sudden infant death syndrome and,
1425-1426
Potassium chloride in intravenous solutions,
243
Potassium iodine for internal radiation contamination,
e699-5
Potocki-Shaffer syndrome,
408t
Poverty,
6,
6f
childhood injury and,
20-21
developmental risk due to,
e6-3
health services children in,
10-11
Powders for skin disorders,
2216
P450 oxidoreductase (POR) deficiency,
1937
Practitioners in international pediatric emergency medicine,
e61-15
Pragmatic language disorder,
118
Pramlinitide acetate,
1977
Prazosin
for systemic hypertension,
1645t
Prealbumin
in malnutrition with chronic diarrhea,
1343t
Preauricular sinuses and pits,
2221
Precision of laboratory tests,
e707-1
Precocious puberty,
1886-1894,
1887t,
e545-1
due to brain irradiation,
1890
familial male gonadotropin-independent,
1893
due to gonadotropin-secreting tumors,
1891
pseudohypoparathyroidism with,
1920
vaginal bleeding with,
1869
Precursor B-cell acute lymphocytic leukemia,
1733t,
1734
Predicative genetic testing,
377
Predispositional genetic testing,
377
Prednisone,
e568-6
for acute rheumatic fever,
923
for autoimmune hepatitis,
1410
for chronic granulomatous disease,
746
and dexamethasone, for cancer therapy,
e488-4t
for Duchenne and Becker muscular dystrophy,
2122
for Henoch-Schönlein purpura,
870
for idiopathic thrombocytopenic purpura,
1717
for inflammatory bowel disease,
1299
for lupus nephritis,
1788
for systemic lupus erythematosus,
844
Preeclampsia,
e89-2t
maternal diabetes mellitus and,
545
Prefixes denoting decimal factors,
e708-1t
Pregnancy
acute intermittent porphyrias and,
e85-8
adolescent,
699-702,
e87-1
characteristic of teen parent in,
700-701
clinical manifestations of,
700
counseling and initial management of,
700
health care for parents and children in,
702t
medical complications of mothers and babies in,
701
psychosocial outcomes/risk for mother and child in,
701-702
asthma treatment during,
801
congenital heart disease and,
1609
dysmenorrhea during,
691t
folic acid supplementation during,
2001
group B streptococci colonization during,
925-926
isotretinoin contraindication during,
2325
obesity prevention during,
187t
prenatal diagnosis and prevention during,
379
psychologic changes in parents during,
e6-8
psychologic stress during,
e6-9
radiation exposure during,
548
in women with hyperphenylalaninemia,
420
Pregnancy-associated plasma protein-A (PAPP-A),
402-403
Pregnancy-related factors in sudden infant death syndrome,
1424-1425
Preimplantation genetic diagnosis (PGD),
381
Prekallikrein (PK)
reference values for,
1698t
Premature atrial contraction (PAC),
1612,
1612f
Premature Infants in Need of Transfusion (PINT) study,
614
Premature labor
group B streptococci prophylaxis in,
640f
Premature rupture of membrane (PROM),
551t,
e89-3-e89-4
group B streptococci prophylaxis in,
641f
Prematurity/premature infant,
555-564
definitions associated with,
555
drug metabolism immaturity in,
562,
563t
electrocardiography of,
1539f
gestational age at birth assessment in,
557,
558f
in high-risk pregnancies,
e89-1
idiopathic apnea of prematurity,
580-581
infection prevention in,
562
pain perception and effects of pain in,
373
physiologic anemia of,
1654
predicting mortality of,
563
sudden infant death syndrome in,
1428
in teenage pregnancy,
701
total parenteral nutrition for,
560
transportation of in motor vehicles,
22
vitamin E deficiency in,
e49-1
vitamin requirements for,
562
Premenstrual dysphoric disorder,
691,
692t
Premyocardial cells,
1527
Prenatal diagnosis,
380t,
381,
e89-2
of erythroblastosis fetalis,
617
genetic counseling in,
378
Prenatal factors in maternal-infant attachment,
e7-1,
e7-1t
Prepuce, newborn assessment of,
536,
536t
Preschool child
behavioral and psychosocial assessment of,
56
child restraint in motor vehicles for,
21t
developmental dysfluency in,
122,
122t
drowning or submersion injury to,
342
growth and development of,
33-36
emotional and moral,
35-36
language, cognition, and play,
34-35
intellectual disability in,
125t
leading causes of death for,
5t
response to death of,
e16-3
Prescription drug abuse, adolescent,
673t
Presenting in psychiatric diagnostic evaluation,
58
Preseptal cellulitis,
2183
Haemophilus influenzae in,
942
Preservatives in immunizing agents,
883
Pressure gradient in breathing,
e365-3
Pressure-induced urticaria and angioedema,
813
Pressure load, cardiac lesions in increased,
1550
Pressure-regulated volume control mechanical ventilation,
325-326
Pressure support ventilation (PSV),
325
Preventive health care,
13-25
in behavioral and mental health issues,
16
family and community in,
16-17
in infancy and early childhood,
16
for injury control,
17-25
in middle childhood and adolescence,
16
quality improvement of,
16
strength-based approaches and framework for,
16
Prick skin test in food adverse reactions,
822
Primary angiitis of central nervous system (PACNS),
876
Primary care physician (PCP), role in emergency medical services,
e61-1
Primary complex in tuberculosis,
998,
1002
Primary effusion based lymphoma (PEL),
1121
Primary pigmented nodular adrenocortical disease (PPNAD),
1939-1940
Primidone
adverse effects of,
2031t
Primitive neuroectodermal tumor (PNET),
1751,
1765
Primitive reflexes assessment in neurologic examination,
e584-7-e584-8
Prion in transmissible spongiform encephalopathies,
1177
PRKCSH gene defect,
1383t
Probiotics
for atopic dermatitis,
805
for inflammatory bowel disease,
1299
Procainamide
for pediatric resuscitation and arrhythmias,
294t
Procaine penicillin G,
645t
for neonatal infection,
645t
Procedures for emergency departments,
e61-4t
Process improvement,
e2-1t
Prochlorperazine
for chemotherapy-associated vomiting,
1244t
Proctocolitis, food protein-induced,
821
Produce-associated salmonellosis,
949-950
Product modification for injury prevention,
19-20,
20t
Product multiplicity,
e56-4
Professional organizations,
12
international pediatric emergency medicine,
e61-12t
Progesterone contraceptives for special needs girls,
1875
Progesterone intrauterine devices (IUDs) for special needs girls,
1875
Progestin for amenorrhea,
688t
Progestin implant for special needs girls,
1875
Prognostic subgroups in cancer diagnosis and staging,
e488-1
Progressive external ophthalmoplegia (PEO),
2067-2068
Progressive familial intrahepatic cholestasis (PFIC),
1383-1384,
1384t
Progressive rubella panencephalitis (PRP),
1077
Progressive systemic sclerosis,
e637-5
Prohormones for performance enhancement,
2423
Prokinetic agents for gastroesophageal reflux disease,
1268
Prolidase deficiency,
443
Proline
genetic disorders of,
445t
Prone positioning, sudden infant death syndrome and,
1425
Pro-opiomelanocortin deficiency,
182t
Propane, as inhalant,
681t
Properdin deficiency,
754t,
755
fever without a focus in,
896t
Prophylaxis
animal and human bite,
2456t
bacterial meningitis,
2095
Haemophilus influenzae type B,
943
measles, postexposure,
1075
neonatal gonococcal,
1037
respiratory syncytial virus,
1129
ureteropelvic junction obstruction,
1841-1842
Propionibacterium acnes,
2322
Propionyl CoA carboxylase deficiency,
436-437
Propranolol
for congenital hypothyroidism,
1913
for migraine prophylaxis,
2044t
for systemic hypertension,
1645t
for tetralogy of Fallot,
1576
for vomiting prophylaxis,
1244t
Proprotein convertase 1/3 deficiency,
1312
Propylthiouracil (PTU)
for congenital hypothyroidism,
1913
Prospective memory,
e29-3
Prostaglandin E
1
for cardiogenic shock,
313t
for tetralogy of Fallot,
1576
for transposition of great arteries with ventricular septal defect and pulmonary stenosis,
1582-1583
for tricuspid atresia,
1581
Prostaglandins
in neuroendocrine tumor-associated diarrhea,
e333-2t
possible adverse reactions to in premature infant,
563t
Prosthesis
orthopedic, infection associated with,
e172-3
Prostigmine methylsulfate, in myasthenia gravis diagnosis,
2134
Protamine, as poisoning antidote,
258t
Protease-resistant proteins (PrP) in transmissible spongiform encephalopathies,
1177,
e270-1-e270-2
Protective factors for abuse and neglect,
136-137
Protein(s)
in acute renal failure,
1820t
adequate macronutrient distribution range for,
e41-1t
digestion and absorption of,
e320-1
familial intolerance of,
455
Protein A,
Staphylococcus aureus production of,
904
Protein AT deficiency,
1708
Protein C
reference values for,
1698t
Protein hydrolysate formula,
164
Protein S
reference values for,
1698t
Proteins induced by vitamin K absence (PIVKA),
210
Protein tyrosine inhibitors for cancer,
e488-2t
Proteus syndrome myopathy,
2119
Prothrombin time (PT)
in hemostatic disorders,
1697
reference values for,
1698t
Protocols for emergency departments,
e61-4t
Proton magnetic resonance spectroscopy (MRS),
e584-11
Proton pump inhibitors (PPIs)
for gastroesophageal reflux disease,
1268
for
Helicobacter pylori gastritis,
1293t
for peptic ulcer disease,
1294
Protoporphyrinogen oxidase (PPO),
e85-2f
Protozoan disease
Cyclospora cayetanensis,
1184
Provocation paralysis, due to poliovirus infection,
1083
Provocation testing in allergic disease,
768
Proximal humeral fracture,
2392
Proximal tubule in acid-base balance,
e52-14
Pruritus
in atopic dermatitis,
802
as manifestation of liver disease,
1377t
Prussian blue for internal radiation contamination,
e699-5
Pseudodominant inheritance,
388,
388f
Pseudo-Hurler polydystrophy,
491-492
Pseudohyperparathyroidism,
1920
Pseudohypertrophy assessment in neurologic examination,
e584-6
Pseudohypoaldosteronism type 1,
221
Pseudohypoaldosteronism type 2,
221
Pseudomembranous conjunctivitis,
2168
Pseudomonas maltophilia,
e197-2
Pseudoparalysis
due to osteomyelitis,
2395
Pseudo-status epilepticus,
2038
Pseudotumor, orbital,
2182
Pseuoparalysis of Parrot,
1018
Psychiatric disorders,
57t
disruptive behavioral disorders as,
96-100,
97t
eating disorders as,
90-96
definitions associated with,
90,
90t
differential diagnosis,
91
laboratory findings in,
91
habit disorders as,
75-76
language disorders as risk factor for,
121
mood disorders as,
82
dysthymic disorder,
87,
87t
office intervention for,
16
rumination disorder as,
70-71
Tourette’s syndrome as,
77
Psychiatric hospitalization,
66
Psychoanalytical theories of development,
e6-3-e6-4
Psychodynamic psychotherapy,
66
Psychogenic eye disturbances,
2154
Psychogenic movement disorders,
2061
Psychogenic nonepileptic seizures,
e587-2
Psychologic adjustment to burn injury,
355
Psychological complications
of sickle cell disease,
1669
of type 1 diabetes mellitus,
1986
Psychological factors affecting general medicine conditions,
67
“Psychological First Aid”,
e36-7
Psychological support following traumatic injury,
340
Psychologic evaluation
in communication disorders,
120
in renal transplantation,
e530-3
Psychologic influences
on neurodevelopmental dysfunction,
e29-1
Psychologic stress
in psychosomatic illness,
68
type 1 diabetes mellitus development and,
1972
Psychosis
due to glucocorticoid excess,
e568-5
psychopharmacologic management of,
61t
Psychosocial assessment of adolescent,
666,
666t
Psychosocial causes of hypopituitarism,
1881
Psychosocial consequences
Psychosocial development during adolescence,
654
Psychosocial issues
in juvenile idiopathic arthritis,
839
Psychotherapy,
65-66
for grief and loss,
e16-5
for neurodevelopmental dysfunction,
e29-8
PTC124 for cystic fibrosis,
1493
Pten hamartoma tumor syndrome (PTEN),
e337-2
Ptosis,
2163
in neuromuscular disorders,
2115t
P53 tumor suppressor gene, mutations,
1914,
e486-1
Puberty
See also Adolescent, growth and development of
precocious,
1886-1894,
1887t,
e545-1
due to brain irradiation,
1890
familial male gonadotropin-independent,
1893
due to gonadotropin-secreting tumors,
1891
due to McCune-Albright syndrome,
1892f
pseudohypoparathyroidism with,
1920
vaginal bleeding with,
1869
timing of onset,
649
secular trend for decreasing age of,
649
Pubic hair, sexual maturity ratings of changes in,
651f
Pulmonary abscess,
1480-1481
clinical manifestations of,
1480
pathology and pathogenesis of,
1480
Pulmonary agenesis and aplasia,
1463
Pulmonary air embolism,
597
Pulmonary arteriography,
e366-3
Pulmonary artery
absence of branch, with tetralogy of Fallot,
1576
in fetal circulation,
1529
Pulmonary artery sling,
1452
Pulmonary aspiration, due to drowning,
343
Pulmonary blood flow, cyanotic congenital heart disease and,
1573-1596
Pulmonary hypoplasia,
1464
with congenital diaphragmatic hernia,
594
due to oligohydramnios,
e89-2
Pulmonary infiltrates with eosinophilia (PIE),
1474
Pulmonary interstitial emphysema (PIE), neonatal,
597-599,
598f
Pulmonary lymphangiectasia, congenital,
1467
Pulmonary lymphatic compartment, pulmonary edema and,
1468
Pulmonary sequestration,
1465,
1466f
in partial anomalous pulmonary venous return,
1553-1554
Pulmonary therapy for cystic fibrosis,
1491-1493
Pulmonary valve
congenital absence of,
1571
with tetralogy of Fallot,
1576
rheumatic disease of,
1628
Pulmonary valve stenosis
double-outlet right ventricle with,
1588
infundibular
and double chamber right ventricle,
1564
ventricular septal defect with,
1558
intracardiac shunt with,
1564
transposition of the great arteries and ventricular septal defect with,
1574,
1583f
Pulmonary valvular insufficiency,
1571
Pulmonary vascular pressure, pulmonary edema and,
1468
Pulse(s)
in coarctation of the aorta,
1568
Pulse oximetry
in respiratory distress and respiratory failure,
318
Pulse rate in asthma,
784t
Puncture wounds of foot,
2341
Purine nucleoside phosphorylase (PNP) deficiency,
733
Purpura fulminans in meningococcal disease,
931-932
Purpuric rash in rheumatic disease,
e147-2t
Purtscher retinopathy,
2180
Purulent pericarditis,
1636
Pustular folliculitis, eosinophilic,
2220
Pyelogram, antegrade,
1841
Pyoderma gangrenosum in PAPA syndrome,
858-859
Pyogenic arthritis, pyoderma gangrenosum, and acne (PAPA) syndrome,
858-859
Pyomyositis,
Staphylococcus aureus in,
905
Pyridostigmine bromide for myasthenia gravis,
2135t
Pyridoxal phosphate for epilepsy,
2028
Pyriform aperture stenosis,
1431
Pyrimidine 5’-nucleotidase deficiency,
e83-8-e83-9
overactive cytosolic 5’-nucleotidase and,
e83-9
Pyruvate carboxylase deficiency,
494t-495t,
506
secondary to holocarboxylase synthetase or biotinidase,
506
Pyuria
in urinary tract infection,
1831
R
Rabson-Mendenhall syndrome,
1996
Racial and ethnic factors
in adolescent drug use,
672
in childhood cancers,
1727t
in childhood injuries,
20
in cleft lip and palate,
1252
in developmental dysplasia of the hip,
2356
in Familial Mediterranean fever,
856
in infant mortality rates,
e87-2f
in sexually transmitted disease,
705,
706f
Racial minority children,
6-7
Radial-femoral delay,
1532-1533
in coarctation of the aorta,
1568
Radiation exposure
as cancer risk factor,
1727t
in thyroid carcinoma,
1914
microcephaly due to,
2007t
Radiation heat loss in newborn,
536-537
Radiation therapy
to brain, precocious puberty due to,
1890
as cancer risk factor,
1727t
in thyroid carcinoma,
1914
hypogonadism due to,
1945
hypothyroidism due to,
1901
total body, late effects of,
e133-1
Radioactive iodine for Graves disease,
1912t
Radiocontrast media, adverse reaction to,
828
Radiography
in congenital vertical talus,
2338
in disk space infection,
2376
in fever of unknown origin,
902
in gastroesophageal reflux disease,
1267,
1267f
in juvenile idiopathic arthritis,
836,
837f
in liver dysfunction,
1379
in neonatal necrotizing enterocolitis,
602,
602f
in pulmonary embolism,
1502
in respiratory distress syndrome,
582,
583f
in skeletal dysplasias,
e685-2
in talipes equinovarus,
2337
in total anomalous pulmonary venous return,
1589,
1590f
Radioiodine administration
hypothyroidism due to,
1896
Radioisotope studies in urinary tract obstruction,
1840-1841
Radionuclide studies
in aspiration syndromes,
1472t
in fever of unknown origin,
902
in pulmonary embolism,
1502
in septic arthritis,
2400
Rage attack, seizure
versus,
e587-4
Ragged red fibers, myoclonus epilepsy and,
2067
Ramipril for systemic hypertension,
1645t
Ranitidine
for
Helicobacter pylori gastritis,
1293t
for urticaria and angioedema,
815t
Rapid antigen detection
in bacterial and fungal infection diagnosis,
e164-1
in group A streptococci infection,
917-918
in parainfluenza viruses,
1125t
Rapid eye movement (REM), respiratory regulation in,
e365-14
Rapidly involuting congenital hemangioma (RICH),
2229
Rapid-onset with hypothalamic dysfunction, hypoventilation, and autonomic dysregulation (ROHHAD),
1521-1522
Rapid sequence intubation (RSI),
285,
287t
Rash
of Henoch-Schönlein purpura,
869,
869f
due to neonatal infection,
639
of systemic-onset juvenile idiopathic arthritis,
832-834,
834f
of varicella-zoster virus infection,
1105,
1105f
Rashkind balloon atrial septostomy,
1586,
1586f
Rasmussen’s encephalitis,
2023
Rating scales, mental health,
57,
57t
RB tumor suppressor gene, inactivation of,
e486-1
Reactive airway disease, gastroesophageal reflux disease with,
1263
Reactive fetal heart rate (FHR),
543t
Reactive perforating collagenosis (RPC),
2279,
2279f
Ready to use therapeutic foods (RUFTs),
177,
177f
Real-time continuous glucose monitoring (RT-CGM),
1983-1984
Real-time polymerase chain reaction (RT-PCR),
e164-5
in enterovirus infection,
1093
in respiratory syncytial virus infection,
1128
“Rebound” hypertension,
1569
Recessive dystrophic epidermolysis bullosa (RDEB),
2246,
2247f
Recessive X-linked ichthyosis,
2268t
Recognition recall,
e29-3
Recombinant growth factor
for Turner syndrome,
1954
Recombinant insulin-like growth factor-1,
1881
Recombinant tissue plasminogen activator (rTPA),
1712
Recombinase activating genes 2
(RAG-2),
e117-1
Recombinase activating genes 1
(RAG-1) deficiency,
732-733
Recommendations for Preventive Pediatric Health Care,
14,
15f
Reconstruction for burn injury,
355
Recreational activity, drowning during,
342
Recrudescence in malaria,
1201
Recruitment, alveolar,
323
Rectal examination
in fever of unknown origin,
901
Rectal suction biopsy in Hirschsprung disease,
1285-1286
Rectal swab culture
in
Campylobacter infection,
970
in
Shigella infection,
960
Rectobulbarurethral fistula,
1357
Rectoprostaticurethral fistula,
1357
Red blood cells (RBCs)
life span of in fetus and neonate,
e440-6
morphologic abnormalities of,
1650f
reduction of hemoglobin concentration of
See (Anemia(s))
Red blood cells (RBCs) count
in iron deficiency-anemia,
1656t
from 18 weeks of gestation to 14 weeks of life,
613t
Red cell distribution width (RDW)
in congenital dyserythropoietic anemia,
e446-1t
in iron deficiency-anemia,
1656t
Red cherry spot, macular,
483
Red eye, differential diagnosis of,
2167t
Reduviid insects in trypanosomiasis,
1195
Reed-Sternberg (RS) cell,
1740
Referral
psychiatric disorders,
58
Reflex(es)
brainstem, brain death and,
e63-2
tendon,
2109
in hypoxic-ischemic encephalopathy,
571t
Reflex sympathetic dystrophy,
2143
Reflux-related renal injury,
1834
Refractory anemia with excess of blasts (RAEB),
758-759
Refractory status epilepticus,
2038
Registration, Evaluation, Authorization, and restriction to Chemicals (REACH) legislation,
e700-1
Regulation, child care,
e15-1
Rehabilitation
following heart transplantation,
e437-4
for sports-related ankle injury,
2418
Rehabilitation model in psychosomatic illness,
70
Rehydration therapy
for rotavirus, calcivirus, and astrovirus gastroenteritis,
1136
Rejection
of hematopoietic stem cell transplantation,
760-762
of renal transplantation,
e530-5
Relapsing
of acute lymphocytic leukemia,
1736
of Hodgkin lymphoma,
1743
of nephrotic syndrome,
1805
Relationships, adolescent development of,
652-654
Relative bioavailability in drug therapy,
e57-3
Relative rest following sports injury,
2408
Relaxation
transient lower esophageal sphincter,
e310-1
gastroesophageal reflux disease and,
1266
Reliability
in quality measurement,
e2-2t
Remifentanil for anesthesia,
e70-7
Remission induction,
1734
Remote symptomatic seizure,
2013
Renal biopsy
in renal transplantation,
e530-5
in systemic lupus erythematosus,
842
Renal cell carcinoma (RCC),
1760
Renal disease
See also Nephrology
failure to thrive in,
148t
in type I glycogen storage disease,
495
Renal dysfunction
due to immunosuppression therapy,
e437-3
Renal failure,
1818-1826
cortical necrosis in,
1818
dental problems associated with,
1251t
metabolic acidosis in,
232
Renal scan in urinary tract infection,
1833,
1833f
Renal solute loads, for premature infant,
559
Renal system
glucocorticoids role in,
e568-5
Renal tubular acidosis (RTA),
1808-1811
metabolic acidosis and,
232
urinary lithiasis with,
e541-2
Renal tubules
disorders of
Gitelman syndrome as,
1814
nephrogenic diabetes insipidus as,
1812
renal tubular acidosis as,
1811f
Renal vasculitis, nephrotoxins in,
1817t
Renal vein thrombosis (RVT),
1709
in newborn assessment,
535
Renin-angiotensin system,
e52-5
in aldosterone regulation,
1923
Replacement therapy for genetic disorders,
379-380
Replantation of tooth,
1259
Reproductive factors in high-risk pregnancies,
e89-1t
Research
on emergency medical services for children,
e61-5
international collaborations,
e61-12t
quality improvement and,
e2-5
Reserpine
possible adverse reactions to in premature infant,
563t
for spasticity of cerebral palsy,
2064
Residency Review and Redesign in Pediatrics (R3P),
11
Resistance
bacterial,
e173-1,
e173-1t
Haemophilus influenzae,
941
in neonatal infection,
644
Pseudomonas aeruginosa,
977
Streptococcus pneumoniae,
913
Resorption, bone, disorders involving defective,
2432-2433
Resources,
e61-14t
child care information,
e15-4t
developmental-behavioral screening and surveillance,
40
international, for pediatric emergency medicine,
894t
internet
for pharmacogenetics and pharmacogenomics,
e56-7t
Resperidone for mood stabilization,
64t
Respiration(s)
in newborn
failure to initiate or sustain,
575
transition to pulmonary respiration in,
579-580
Respiratory disease
acute inflammatory upper airway obstruction as,
1445-1450
child care and infections of,
e167-1
chronic severe respiratory insufficiency as,
1519-1526
failure to thrive in,
148t
human papillomavirus,
1138
of newborn,
579-599
foramen of Morgagni hernia as,
597,
597f
foreign material aspiration as,
590,
591f
paraesophageal hernia as,
597
persistent pulmonary hypertension of the newborn as,
592-594,
592f
pulmonary hemorrhage as,
599
respiratory distress syndrome as,
581-590
transient tachypnea as,
590
parenchymal
emergency airway management in,
284
peritonsillar cellulitis/abscess as,
1440,
1442
in premature infants,
559t
psychopharmacology and,
65
sublottic stenosis as,
1454
Respiratory distress,
314
in acutely ill child,
275
advanced airway management techniques for
in congenital diaphragmatic hernia,
595
as delivery room emergency,
575
mechanical ventilation for,
321-329
neurologic disease manifesting as,
316
due to parenchymal lung disease,
284
toxic-metabolic states manifesting as,
316
Respiratory distress syndrome (RDS),
581-590
clinical manifestations of,
582
Respiratory failure,
316,
317f,
317t,
e365-9f
advanced airway management techniques for
due to congenital central hypoventilation syndrome,
1520-1522
as delivery room emergency,
575
follow open heart surgery,
1604
mechanical ventilation for,
321-329
due to parenchymal lung disease,
284
presentation profiles of,
317f
Respiratory insufficiency
due to congenital central hypoventilation syndrome,
1520-1522
infections associated with,
1525
due to myelomeningocele with Arnold-Chiari type II malformation,
1522
due to neuromuscular diseases,
1520t
due to obesity hypoventilation syndrome,
1522-1523
due to obstructive sleep apnea,
1523
due to spinal cord injury,
1523
Respiratory manifestations,
e413-1,
e413-1t
in gastroesophageal reflux disease,
1269
in lysosomal storage disorders,
485t
in multiple organ dysfunction syndrome,
312t
in Niemann-Pick disease,
488
in setting of tearooms,
e704-8
in systemic inflammatory response syndrome,
309t
in systemic lupus erythematosus,
843t
in systemic scleroderma,
851
Respiratory rate
in respiratory distress,
315t
Respiratory secretions treatment in palliative care,
155t-156t,
157
Respiratory system
management of in drowning,
345
poliovirus infection effects on,
1084
shock-related dysfunction of,
307t
Respiratory tract infections
group A streptococcus in,
916
Staphylococcus aureus in,
905
Rest following sports injury,
2408
Restless legs syndrome (RLS),
52-53
Restless leg syndrome (RLS)
Restrictive dermopathy,
e84-2t
Resuscitation
infection protection and control in,
e166-2t
Reticular dysgenesis,
733
Reticulocytes, in congenital dyserythropoietic anemia,
e446-1t
Reticulocyte hemoglobin content in iron deficiency-anemia,
1656t-1657t
Reticuloendothelial sequestration,
749
Retina
disorders of,
2174-2181
Best vitelliform degeneration as,
2178
with blood disorders,
2180
coloboma of the fundus as,
2181
familial exudative vitreoretinopathy as,
2179
myelinated nerve fibers as,
2181
persistent fetal vasculature as,
2176
retinal detachment as,
2179
Stargardt disease as,
2178
with subacute bacterial endocarditis,
2180
neurologic examination of,
e584-2
Retinal hemorrhage
neurologic examination of,
e584-3
Retinoblastoma gene,
1768
Retinoblastoma protein,
1768
Retinoids
for pityriasis rubra pilaris,
2263
Retinol-binding protein (RBP),
188
in malnutrition with chronic diarrhea,
1343t
Retinopathy
due to cat-scratch disease,
985
salt-and-pepper, due to congenital rubella syndrome,
1077-1078
in subacute bacterial endocarditis,
2180
Retractions in respiratory distress,
315t
Retrocochlear hearing loss,
2188
Retrograde pyelogram,
1841
Retropharyngeal space infection,
1444
Reunion, child’s response to,
e16-1
Reverse transcription polymerase chain reaction (RT-PCR),
1155
Reversible infantile cytochrome C oxidase deficiency myopathy,
2066-2067
Rhabdoid tumor of kidney (RTK),
1760
Rhabdomyolysis
due to hypophosphatemia,
228
Rh deficiency syndrome,
e454-1
Rhesus-associated glycoprotein (RHAG),
e454-1
Rheumatic disease
ankylosing spondylitis and other spondyloarthritides as,
e150-1-e150-3
fever of unknown origin in,
900t
hereditary periodic fever syndromes as,
855-860,
855t-856t
chronic infantile neurologic cutaneous and articular disease as,
858
familial cold autoinflammatory syndrome as,
858
hyperimmunoglobulinemia D syndrome as,
857-858
Muckle-Wells syndrome as,
858
periodic fever, aphthous stomatitis, pharyngitis, and adenitis as,
859-860
pyogenic arthritis, pyoderma gangrenosum, and acne syndrome as,
858-859
tumor necrosis factor receptor-associated periodic syndrome as,
858,
859f
hypertrophic osteoarthropathy as,
e163-1
juvenile dermatomyositis as,
846-850
juvenile idiopathic arthritis as,
829-839
Mucha-Habermann disease as,
e163-1
Raynaud phenomenon as,
852
reactive and postinfection arthritis as,
839-841
systemic lupus erythematosus as,
841-846
vasculitis syndromes as,
867-876,
868t,
876t
antineutrophil cytoplasmic antibodies (ANCA)-associated vasculitis as,
874-876
polyarteritis nodosa and cutaneous polyarteritis nodosa as,
872-874
Rheumatoid arthritis, acute rheumatic fever
versus,
923,
923t
Rhinitis medicamentosa,
1435
Rhinoconjunctivitis, food-induced,
822
Rhinorrhea
in respiratory syncytial virus infection,
1128
Rhinosinusitis in cystic fibrosis,
1496
Rhododendron toxicity,
269t
Rhythmic movements, sleep-related,
52-53
Ribs
notching of inferior border of,
1568
RICE treatment for ankle sprains,
2418
Rickets,
e694-2,
e694-2t
autosomal dominant hypophosphatemic,
207
due to calcium deficiency,
206
due to Fanconi syndrome,
207
hereditary hypophosphatemic with hypercalciuria,
207
due to phosphorous deficiency,
206-207
due to renal tubular acidosis,
208,
1811
vitamin D-dependent
dental problems associated with,
1251t
due to vitamin D disorders,
204-206
Riedel’s thyroiditis,
1904t
Rifampin,
e173-13,
e206-1-e206-2
adrenal insufficiency due to,
1927
for bacterial meningitis,
2093t
for epiglottitis prophylaxis,
1448
for
Neisseria meningitidis prophylaxis,
934t
for neonatal infection,
645t
for
Staphylococcus aureus,
907t
Right ventricle
double-outlet,
1582
with malposition of great arteries,
1588-1589
with pulmonary stenosis,
1588
Rigid endoscopy in sinusitis,
1437
Rigidity, muscle, assessment in neurologic examination,
e584-6
Riley-Day syndrome
cardiac manifestations of,
1531t
Ring form of
Plasmodium,
1199
Ring(s)
vaginal contraceptive,
697
special needs girls and,
1875
Risk factors
for abuse and neglect,
136
for adolescent drug use and abuse,
672
for adverse drug reactions,
825
for childhood cancers,
1727t
for childhood injuries,
20-21
for developmental dysplasia of hip,
2356-2357
for disruptive behavioral disorders,
98
for major depression,
83-84
for psychosomatic illness,
67-68
for school violence,
e36-3
for type 2 diabetes mellitus,
1991
Risperdal
See Resperidone; Risperidone
Risperidone
for pain management,
364t
for psychosis and agitation,
64t
Rituximab
for juvenile idiopathic arthritis,
838t
Rizatriptan for migraine,
2044t
Rocuronium for intubation,
321t
Rome III criteria for diagnosis of functional abdominal pain,
1346,
1347t
Rome Statute of the International Criminal Court,
e36-6
Rosary
due to vitamin C deficiency,
198,
199f
Rotator cuff impingement syndrome,
2410
Rotator cuff injury,
2410
Rotavirus vaccine,
884t,
1137
in gastroenteritis prevention,
1338
immunocompetence and,
891
recommended schedule for,
887f,
889
Rubella,
1075-1078
arthritis associated with,
840
congenital heart disease with,
1531t
differential diagnosis of,
1077
exclusion from day care due to,
e15-2t
laboratory findings in,
1076
maternal
fetal and neonatal effects of,
e89-3t
supportive care for,
1078
in type 1 diabetes mellitus development,
1971
Rufinamide
adverse effects of,
2031t
Rumack-Matthew nomogram for acetaminophen poisoning,
259,
259f
Rumination disorder,
70-71
Runaway and thrown-away children,
8
Runner’s hyponatremia,
1885
Rupture, esophageal,
1271
Rural-urban location, childhood injuries and,
20-21
S
Sabin-Feldman dye test,
1213
Sacral agenesis,
2118
neuropathic bladder and,
e536-3
Saddle nose deformity
in Wegener’s granulomatosis,
874,
875f
Saethre-Chotzen syndrome,
2012t
Safety World Inventory and Literacy Screener (SWILS),
41t-43t
Safe zone of Ramsey,
2360f
Saiboku-to for asthma,
271t
Salicylates
for acute rheumatic fever,
923
poisoning with,
253t,
260
metabolic acidosis due to,
233
Saline
hypertonic for cystic fibrosis,
1491
Salivary glands
effects of eating disorders on,
93t
Salmeterol for asthma,
794t
Salmonella enterica serovar Typhi,
954-958
Salmonellosis,
948-958,
949t
enteric (typhoid) fever due to,
954-958
differential diagnosis of,
957
inflammatory bowel disease
versus,
1298t
traveler’s diarrhea due to,
1338t
Salt depletion in cystic fibrosis,
1487,
1496
Salter-Harris fracture,
2408
Salt loss, hyponatremia due to,
1885
Salt poisoning
plasma osmolality in,
e52-3
Salt wasting
renal, hyponatremia due to,
216
Sanitation for gastroenteritis prevention,
1338
Saphenous vein, venous access in,
292,
295f
Saprophytic
Aspergillus syndromes,
1059
Sarcolemma in cardiac development,
1528
Sarcoma
clear cell of kidney,
1760
Kaposi’s
human herpesvirus 8 in,
1121
Sarcoplasmic reticulum (SR), in cardiac development,
e414-4
Sarcoptes scabiei var.
canis,
2320
Sarcoptes scabiei var.
hominis,
2319
Sardonic smile of tetanus,
992
Scales, examination of,
e637-1
Scalp blood, fetal sampling of,
544
Scapulohumeral muscular dystrophy,
2123
Scarlatiniform erythema,
2302
Schimke immunoosseous dysplasia,
748t,
1690
School
chemical pollutants in,
e700-3
chronic illness and,
e39-3
obesity prevention in,
187t
perceptual, cognitive, and language processes required for success in elementary,
37-38,
37t
refusal to attend due to social phobia,
79
School-age child
behavioral and psychosocial assessment in,
56
child restraint in motor vehicles for,
21t
disruptive behavioral disturbances in,
99-100
drowning or submersion injury to,
342
growth and development of,
36-39
social, emotional, and moral,
38-39
injury risk factors for,
20
intellectual disability in,
125t
leading causes of death for,
5t
response to death of,
e16-3
response to divorce of,
e16-1
Scintigraphy
in aspiration syndromes,
1472t
in congenital hypothyroidism,
1900
in neonatal cholestasis,
1385
Sclera, development of,
2148
Scleredema adultorum,
2276
Scleredema of Buschke,
2276
Scleroderma,
850-853
clinical manifestations of,
850-852
etiology and pathogenesis of,
850
laboratory findings in,
853
Sclerosing cholangitis with inflammatory bowel disease,
e352-1
Sclerosis
progressive systemic, cutaneous manifestations of,
e637-5
Scoliosis
associated with pelvic obliquity,
e674-5
idiopathic
etiology and epidemiology of,
2365
Scopolamine
for motion sickness,
1244t
for respiratory secretions in palliative care,
155t-156t
Scorbutic rosary, due to vitamin C deficiency,
198,
199f
Score for Neonatal Acute Physiology (SNAP),
563t
Screening
in acutely ill child evaluation,
277
for child abuse risk factors,
142
major depressive disorders,
84t
Scrotum
examination of in adolescent,
666
newborn assessment of,
536
Seabather’s eruption,
2322
Seasonal allergic conjunctivitis,
809-810
Seasonal allergic rhinitis (SAR),
775
Sebaceous hyperplasia,
2218
Seborrheic blepharitis,
2164
Second-degree heart block,
1618
Second-generation antihistamines,
771,
771t
for urticaria and angioedema,
815t
Second-hand smoke
sudden infant death syndrome and,
1424
Second heart sound, auscultation of,
1533
Second malignancy,
e488-9
after hematopoietic stem cell transplantation,
e133-1
Sedation,
359-360,
e70-16,
e70-16t
in general anesthesia,
e70-1
in mechanical ventilation,
328
for persistent pulmonary hypertension of the newborn,
593
in rapid sequence intubation,
287t
Segregation analysis,
e77-2
Seizures,
2013-2039
in acute intermittent porphyrias,
e85-7
with bacterial meningitis,
2094
dental problems associated with,
1251t
in factitious disorder by proxy,
146
genetic factors in,
2016t
in hypoxic-ischemic encephalopathy,
571t
due to pork tapeworm,
1235
psychogenic nonepileptic,
e587-2
strokelike events
versus,
2085
in X-linked adrenoleukodystrophy,
468
Selective attention,
e29-3
Selective mutism,
79,
118
Selective serotonin reuptake inhibitors (SSRIs),
61
for attention deficit/hyperactivity disorder,
62t
for depression and anxiety symptoms,
63t,
84
maternal use of, neonatal behavioral syndromes due to,
625,
625f
for premenstrual dysphoric disorder,
692t
safety and efficacy concerns about,
82
Self examination of breast,
e545-1
Self-help skill in Down syndrome,
403t
Self-injectable epinephrine
Self-monitoring of blood glucose (SMBG),
1982-1983
Senior-Løken syndrome,
1816
Sensitivity of laboratory tests,
e707-1
Sensory ataxia, gait of,
e584-7
Sensory testing (ST) of esophagus,
e310-3
Separation anxiety disorder (SAD),
77-78
Sepiapterin reductase deficiency,
446
Sepsis
cardiac manifestations of,
1532t
infant botulism
versus,
989
international consensus definitions of,
311t
recurrent, in factitious disorder by proxy,
146
respiratory distress due to,
315t
Staphylococcus aureus,
905
Sepsis syndrome,
Cryptococcus neoformans in,
1057
Septal defect
ventricular,
1556-1558,
1556f-1557f
coarctation of the aorta,
1570
embryonic development of,
1527
supracristal, with aortic insufficiency,
1559
transitional circulation and,
e418-1
transposition of the great arteries,
1587
with transposition of the great arteries and pulmonary stenosis,
1574,
1583f
Septicemia
Staphylococcus aureus,
908
Septicemic leptospirosis,
1024
Septic shock,
307t
clinical manifestations of,
309
hemodynamic variables in,
311t
Septo-optic dysplasia,
527
adrenal insufficiency with,
1929
diabetes insipidus with,
1883
Septostomy, Rashkind balloon atrial,
1586,
1586f
Serial casting for clubfoot,
2337
Serine
defects in metabolism of,
442
genetic disorders of,
445t
Serology,
e164-4
for differential diagnosis,
e707-4
in enterovirus infection,
1093
in fever of unknown origin,
902
in parvovirus B19 infection,
1097
Serosal complement control protein deficiency,
755
Serotonin
genetic disorders of,
445t
in neuroendocrine tumor-associated diarrhea,
e333-2t
Serotonin discontinuation syndrome,
625
Serotyping in
Haemophilus influenzae,
941
Sertoli Cell-only syndrome,
1945
Sertraline
for depression and anxiety symptoms,
63t
for premenstrual dysphoric disorder,
692t
for weight loss in adults,
187t
Serum α-fetoprotein concentration,
543t
Serum agglutination test (SAT)
in group A streptococci infection,
918
Serum thyroxine-binding globulin,
e557-2
Settings of care, palliative,
151
Severe achondroplasia with developmental delay and acanthosis nigricans (SADDAN),
2428
Severe acute respiratory syndrome-associated coronavirus (SARS-CoV),
1134,
e256-3
Severe congenital neutropenia,
750
Sevoflurane for anesthesia,
e70-6
Sex
types and definitions,
654
Sex-hormone binding globulin (SHBG),
e576-1
Sex partner treatment for
Chlamydia trachomatis,
1036-1037
Sexual behavior,
655
trends in prevalence of,
693t
Sexual development,
649
Turner syndrome and,
1953
Sexual education for special needs girls,
1874
Sexual identity
development of,
654-658
factors that influence,
655
gender variance/gender role nonconformity in,
655-656
gender variant identity/transgender children in,
656-658,
657t
Sexuality
special needs girls and,
1874
Sexually transmitted infections (STIs),
705-714
human papillomavirus,
1137
lymphogranuloma venereum as,
1038
as threat to homosexual youth,
659
Shake lotions for skin disorders,
2216
Shaken baby syndrome,
2181f
Shampoo for skin disorders,
2216
Shape of head in neurologic examination,
e584-2
Shiga toxin-producing
Escherichia coli (STEC),
962t,
963
Shigella,
959-961
clinical manifestations and complications of,
960
differential diagnosis of,
960
inflammatory bowel disease
versus,
1298t
Shinipi-to for asthma,
271t
Shock,
305-314See also specific types
Short-acting inhaled β-adrenergic agents (SABAs)
Short-chain acyl CoA dehydrogenase (SCAD) deficiency,
457t,
460
Short-chain fatty acids (SCFAs),
e41-16
Short-chain 3-hydroxyacyl CoA dehydrogenase (SCHAD) deficiency,
457t,
460
Short Q-T syndrome (SQTS),
1617t,
1618
sudden infant death syndrome and,
1426
Short-rib polydactyly syndromes,
2434
Short stature
due to hypothyroidism,
1902f
due to skeletal dysplasia,
e685-1
Short-term memory (STM),
e29-3
Shoulder
arthrogryposis involving,
e674-5
musculoskeletal pain syndrome of,
877t
orthopedic disorders of,
2383
Shprintzen-Goldberg syndrome,
2012t
Shunt
cerebrospinal fluid, infections associated with,
e172-1-e172-2
coagulase-negative staphylococci,
910
Glenn, bidirectional,
1581
transjugular intrahepatic portosystemic,
e359-3
Sibling
hematopoietic stem cell transplantation form,
757-760,
758t
sudden infant death syndrome in,
1428
Sickle cell disease (SCD),
1663-1670
clinical manifestations of,
1663-1669
cognitive and psychological complications,
1669
splenic sequestration,
1664
complement system dysfunction in,
756
fever without a focus in,
896t
gain-of-function mutation in,
e74-3
hematopoietic stem cell transplantation for,
759-760
hepatic dysfunction with,
e352-3
Sick sinus syndrome,
1618
Signal transducers in oncogenesis,
e486-1
Sildenafil for pulmonary hypertension,
1602t
Silver nitrate solutions for burn injury,
353,
353t
Silver sulfadiazine for burn injury,
353,
353t
Simple partial seizure,
2021
Sinding-Larsen-Johansson disease,
2416
Sinecatechins
for human papillomavirus,
1140
Single-photon emission computed tomography (SPECT),
e584-11
Sinus
branchial cleft and thyroglossal,
2221
Sinus tachycardia,
1616t
supraventricular tachycardia
versus,
1613
Sinus venosus atrial septal defect (ASD),
1553
Skeletal dysplasias
achondrogenesis type 1B as,
2431
asphyxiating thoracic dystrophy as,
2434
atelosteogenesis type II,
2431
cartilage-hair hypoplasia as,
2434
hypochondroplasia as,
2430
major problems associated with,
e685-3t
multiple epiphyseal,
2427
short-rib polydactyly syndromes as,
2434
spondylometaphyseal, Kozlowski type,
2435
Skeletal infection
Cryptococcus neoformans in,
1057
nontuberculous mycobacterial,
1012t
Skeletal injuries, due to child abuse,
138,
138t
Skeletal maturation,
e13-4
Skeleton
effects of malnutrition on,
175t
Skew deviation in neurologic examination,
e584-4
Skin
disinfection for blood culture,
e164-1
maintenance water and,
244t
Skin biopsy,
e637-1
in urticarial vasculitis,
814
Skin disorders
of dermis,
2273-2282
corticosteroid-induced atrophy as,
2274
Ehlers-Danlos syndrome as,
2278
elastosis perforans serpiginosa as,
2279,
2279f
reactive perforating collagenosis as,
2279,
2279f
due to infestation
seabather’s eruption,
2322
neurocutaneous,
2046-2053
linear nevus syndrome as,
2052
von Hippel-Lindau disease as,
2052
Skin infections
Blastomyces dermatitidis,
1064
Cryptococcus neoformans in,
1057
human T-lymphocyte-associated,
e269-1
in immigrant children,
134
Pseudomonas aeruginosa,
976t
Staphylococcus aureus in,
905
Skin manifestations,
e637-3-e637-5,
e637-3t
in factitious disorder by proxy,
146
in gastrointestinal disease,
e637-5
in Neonatal Intensive Care Unit Neurobehavioral Scale,
624t
in setting of immunosuppression,
e637-6
Skin testing
Candida, in T-cell function assessment,
720
in food adverse reactions,
822
Skin-to-skin contact for maintenance of newborn body heat,
537
Skull
auscultation of in neurologic examination,
e584-2
palpation in neurologic examination,
e584-2
“Slapped cheek” appearance of fifth disease,
1095,
1095f
Sleep
foreign-born adoptees and,
131
normal developmental changes in,
47t
overweight and obesity and,
182
requirements of,
29f
during 2-6 months of age,
30
sudden infant death syndrome and environment of,
1425
Sleep apnea
with type 2 diabetes mellitus,
1993t
Sleep-disordered breathing (SDB),
49
Sleep disorders,
46-54
attention deficit/hyperactivity disorder
versus,
110
delayed sleep phase disorder as,
53-54
health supervision of,
54,
54t
restless legs syndrome, periodic limb movement disorder, and rhythmic movement as,
52-53
Sleep studies in respiratory disease,
e366-4
Sleep transition disorders,
e587-5
Sleepwear, flame-retardant,
23
Slime layer
of coagulase-negative staphylococci,
909
of
Staphylococcus aureus,
904
Slipped capital femoral epiphysis (SCFE),
2363,
2364f
Slipped vertebral apophysis,
2377
Slit-lamp examination,
2150
Small bowel
bacterial overgrowth in,
1340
Small for gestational age (SGA) newborn
problems associated with,
557t
Small vessel vasculitis, with hepatitis C,
1401
Smile, sardonic, of tetanus,
992
Smith-Magenis syndrome,
408t
Smith-Strang disease,
1319
Smoke, second-hand
sudden infant death syndrome and,
1424
Snapping hit syndrome,
2414
Sn-mesoporphyrin (SnMP), for hyperbilirubinemia,
612
Snow board-related injuries,
23
Soap for skin disorders,
2216
Social anxiety disorder,
78
Social behavior evaluation in communication disorder,
120
Social development
in foreign-born adoptees,
131
during middle childhood,
38
Social effectiveness therapy for children (SET-C),
79
Social history
in neurologic evaluation,
e584-1
Social issues
in children born to teen mothers,
701
regarding homosexuality,
658
Social phobia (SP),
78,
79t
Social support
following traumatic injury,
340
Society, adolescent development of relationships with,
652-654
Socioeconomic factors
in childhood injuries,
20
in
Haemophilus influenzae type b,
940
in high-risk pregnancies,
e89-1t
in psychosomatic illness,
67
Sodium (Na
+),
212-219,
e41-17
hypernatremia due to deficits of,
213,
213t
in oral rehydration solutions,
1335t
retention of in chronic kidney disease,
1823t
supplementation for burn injury,
353
Sodium bicarbonate
for pediatric resuscitation and arrhythmias,
294t
Sodium channel genes, sudden infant death syndrome and,
1425-1426
Sodium channelopathies,
2125t
Sodium cromoglycate for allergic rhinitis,
779
Sodium iodide for thyroid storm,
1912t
Sodium nitroprusside
for cardiac output maintenance and post-resuscitation stabilization,
294t
for hypertensive emergencies,
1646t
Sodium-potassium adenosine triphosphatase (Na
+,K
+-ATPase),
219
Sodium wasting in chronic kidney disease,
1823t
Soft bedding, sudden infant death syndrome and,
1425
Soft tissue infection
nontuberculous mycobacterial,
1013
due to typhoid fever,
957t
Soft tissue sarcoma,
1760-1762
incidence and survival rates for,
1726t
secondary, due to radiation therapy,
e699-5t
Soles, palmoplantar keratodermas of,
2272-2273
Somatic development,
e6-7
Somatoform disorders,
67,
68t
diagnostic criteria for,
68t,
69
Somatosensory amplification,
68
Somatostatin analogs for growth hormone excess,
e554-4
Somatostatin in neuroendocrine tumor-associated diarrhea,
e333-2t
Somatostatinoma, diarrhea caused by,
e333-2t
Sorbitol,
1982
for constipation maintenance therapy,
74t
for fecal disimpaction,
74t
Sore throat in common cold,
1435
Southeast Asian population, cultural values associated with,
e4-1t-e4-2t
Southeastern Asian ovalocytes (SAO),
e453-1
Spaghetti and meatballs appearance of
Malassezia,
e228-1
Spanish-English translation of botanical names,
274t
Spasm(s)
esophageal, diffuse,
1265
Spastic hemiplegia in cerebral palsy,
2062,
2062t
Spasticity assessment in neurologic examination,
e584-6
Spastic quadriplegia in cerebral palsy,
2063
Special cause variation,
e2-4
Specialist referral
psychiatric disorders,
58
Specialization of pediatrics,
12-13
Special needs children,
5-9
abused and neglected children,
135-147
definitions associated with,
135-136
factitious disorder by proxy as,
146-147
foster and kinship care and,
e35-1
United States situation,
136
children in foster and kinship care,
e35-1-e35-3
early childhood trauma and,
e35-1
legislation in USA regarding,
e35-1
children in poverty,
6,
6f
children of immigrants and racial minority groups,
6-7
children of migrant workers,
7
failure to thrive,
147-149
clinical manifestations of,
147
goals of pediatricians regarding,
9
health services for,
10-11
inherent strengths in,
8-9
palliative care for,
149-159,
150f
communication, advanced care planning, and anticipatory guidance in,
151-159,
153t
runaway and thrown-away children,
8
Special Supplemental Nutrition Program for Women, Infants, and Children (WIC),
170
Specific airway resistance,
e366-3
Specific gravity, pleural, in tuberculosis,
1003-1004
Specific language impairment (SLI),
116-118
Spectral karyotyping (SKY),
396
Spectrometry, tandem mass,
e707-2
Speech
in myotonic muscular dystrophy,
2124
Speech-language therapy,
121
Speech-recognition threshold (SRT) in audiometry,
2193
Speech therapy for respiratory insufficiency,
1525
Sphrintzen-Goldberg syndrome,
2444t
Spielmeyer-Vogt disease,
2073
Spinal arteriovenous malformations,
2107-2108
Spinal cord, multiple sclerosis effects on,
2077t
Spinal cord compression
as oncologic emergency,
e488-6t
respiratory distress due to,
315t
spinal arteriovenous malformations as,
2107-2108
Spinal cord injury (SCI),
2106
poliovirus infection
versus,
1085t
respiratory insufficiency due to,
1523
Spinal cord injury without radiographic abnormalities (SCIWORA),
337,
2106
Spinal disorders,
2365-2377,
2365t
intervertebral disk herniation and slipped vertebral apophysis as,
2377
syndromes and genetic disorders,
2371
Spinal dysraphism
congenital scoliosis with,
2369
Spinal fusion for scoliosis
Spinal paralytic poliomyelitis,
1083
Spine
arthrogryposis involving,
e674-5
cervical
juvenile idiopathic arthritis involvement in,
832,
834f
musculoskeletal pain syndrome of,
877t
SPINK gene mutation,
1373
Spinocerebellar ataxia (SCA),
2057t
Spiramycin for toxoplasmosis,
1215
Spiritual issues, grief and,
e16-5
Spirometra mansonoides,
1232t
Spirometry
in pulmonary function testing,
e366-3
Spironolactone
for familial male gonadotropin-independent precocious puberty,
1893
for systemic hypertension,
1645t
Splash burn, due to child abuse,
138
Spleen
anatomy and function of,
1723
Splenic aspiration in leishmaniasis,
1189
Splenic sequestration in sickle cell disease,
1664
Splinter hemorrhages of nails,
2295
Splinting for clubfoot,
2337
Splitting of 2nd heart sound,
1533
Spondylocostal dysostosis syndromes,
e102-2t
Spondyloepiphyseal dysplasias (SED),
2424-2425,
2424f
Kniest dysplasia as variant of,
2425
Spondylometaphyseal dysplasia, Kozlowski type,
2435
Spongiosis in atopic dermatitis,
801
Spontaneous breathing trial (SBT),
329
Spontaneous pneumothorax,
1509
Sporotrichoid nocardiosis,
e183-1
Sports
classification by contact,
2406t
female athlete triad and,
686
sickle cell trait and,
1671t
Sports injuries
in basketball and volleyball,
e684-2
differential diagnosis of,
2408
initial evaluation of,
2407
Sports medicine
menstrual problems and osteopenia in,
2421-2422
Spurious hyperkalemia,
219
Sputum culture in tuberculosis,
1003
Squamous intraepithelial lesion
Stabilizers in immunizing agents,
883
Staging
of graft
versus host disease,
761t
Stains, for microscopic examination,
e164-1t
Staphylococcus aureus,
904-908
atopic dermatitis and,
806
clinical manifestations of,
905-906
differential diagnosis of,
906,
906f
in infective endocarditis,
1622
methicillin-resistant,
907t
in septic arthritis,
2398
with varicella-zoster virus,
1109
Starvation ketoacidosis,
232
State child care licensing,
e15-1
State Children’s Health Insurance Program (SCHIP),
10
Static compliance (C
STAT) assessment in mechanical ventilation,
328
Station, neurologic examination of,
e584-9
Steady state in drug therapy,
e57-3
Steatocrit in chronic diarrhea,
1344t
Steatohepatitis, nonalcoholic,
1408
Stellae ganglion block,
373
Stellate macular retinopathy,
985
Stem cell factor (SCF), fetal,
e440-1t
Stem cells
differentiation into cardiac cells,
1527-1528
Stent, intravascular,
1548,
1548f
for coarctation of the aorta,
1569
Sterile pyuria in urinary tract infection,
1831-1832
Sternal fracture, due to child abuse,
138
Sternocleidomastoid (SCM) muscle,
e584-5
Steroids
diabetes associated with,
1997
panniculitis due to,
2283
Steroid-sparing immunosuppressive drugs,
844-845
Stewart-Prower factor,
1696t
Stimulants
for attention deficit/hyperactivity disorder,
62t,
111-112
cardiac evaluation before administration of,
112f
for psychiatric disorders,
61,
62t
Stinging papule in dracunculiasis,
1227
Stochastic effects of radiation,
2448
Stomach
disorders of
eosinophilic gastroenteritis as,
1304
gastric duplication as,
1276
hypertrophic gastropathy as,
1276
fetal ultrasound of,
550t
Stool(s),
e297-1
blood in, exclusion from day care due to,
e15-2t
rapid antigen detection of,
e164-1
Stool culture,
e164-2-e164-3
in
Campylobacter infection,
970
in
Clostridium difficile infection,
995
in
Shigella infection,
960
Storage of vitamin A,
188
Strabismic amblyopia,
2152
Stramonium folium, potential toxicity of,
272t-273t
Strangulated hernia,
1365
Strawberry tongue in Kawasaki disease,
863,
864f
Strength-based approaches to well child care,
16
Strengths, inherent, in special risk populations,
8-9
Streptococcal toxic shock syndrome,
909,
919
Streptococci
arthritis associated with,
840
group A,
914-925
differential diagnosis of,
918
in toxic shock syndrome,
909
with varicella-zoster virus,
1109
Streptococcus mutans in dental caries,
1255
Streptococcus pneumoniae,
910-914
in bacterial meningitis,
2087
in diarrhea-associated hemolytic-uremic syndrome,
1791-1793
neonatal sepsis due to,
636t
predisposition to infection due to immunodeficiency,
716t
rapid antigen detection of,
e164-1
Streptokinase for empyema,
1509
Stress, psychologic
in psychosomatic illness,
68
type 1 diabetes mellitus development and,
1972
Stretch receptors in respiration regulation,
1421
Strictures, urethral,
1847
Stridor
due to gastroesophageal reflux disease,
1269-1270
as sign of respiratory pathology,
1420
ST segment abnormalities,
1540
Subacute necrotizing encephalomyelopathy,
506-509
Subarachnoid hemorrhage (SAH)
emergency management of,
304
Subcapsular hematoma,
578
Subcutaneous emphysema,
1462
Subcutaneous immunoglobulin (SCIG) for B-cell defects,
727-728
Subcutaneous nodules
in acute myeloid leukemia,
1737
in acute rheumatic fever,
922
Subdural hematoma, due to child abuse,
139
Subdural hemorrhage in newborn,
566
Subgaleal hemorrhage,
565
Subglottic stenosis,
1451
Sublingual immunotherapy (SLIT),
774
Substance abuse
attention deficit/hyperactivity disorder
versus,
110
maternal
fetal and neonatal effects of,
e89-2t
sudden infant death syndrome and,
1424
serotonin syndrome and,
265t
Substitution, genetic,
e74-2
Substrate specificity,
e56-4
Subtle neonatal seizure,
2034
Subungual exostosis,
2343
Subvalvular stenosis,
1565
Succimer
for arsenic and mercury intoxication,
e701-4
Succinic semialdehyde dehydrogenase deficiency,
447
Succinimides, adverse effects of,
2031t
Succinyl CoA:3-ketoacid CoA transferase (SCOT) deficiency,
435,
462
Sucking chest wound,
336t
Sucrase-isomaltase deficiency,
1318
Sucrose for pain management,
364t
Sudden infant death syndrome (SIDS),
1421-1429
in child-care settings,
e15-3
clinical strategies for prevention of,
1428-1429
infant groups at increased risk for,
1428
risk factors for
genetic and environmental interactions in,
1427,
1427f
Sufentanil, equianalgesic doses and half-life of,
367t
Sulfasalazine
for juvenile idiopathic arthritis,
838t
for spondyloarthritides,
e150-2
for urticaria and angioedema,
815t
Sulfatase, multiple deficiency of,
490
Sulfisoxazole,
e173-4t-e173-11t
for acute rheumatic fever prophylaxis,
924t
possible adverse reactions to in premature infant,
563t
Sulfite oxidase deficiency,
429
Sulfur granules in actinomycosis,
e182-1
Superior vena cava syndrome,
e488-6t
Supernumerary teeth,
1430
Supine positioning, sudden infant death syndrome and,
1425
Supplements
vitamin, nutritional aspects of,
169
Support, social
following traumatic injury,
340
Supportive psychotherapy,
66
Suppositories,
74t
for constipation maintenance therapy,
74t
Suppurative arthritis,
942
Supracristal ventricular septal defect with aortic insufficiency,
1559
Supratentorial primitive neuroectodermal tumors (SPNETs),
1752
Supravalvular stenosis,
1565
Surfactant
prophylactic administration of,
585
Surgery
for ambiguous genitalia,
1935
for aortic aneurysm in Marfan syndrome,
2445
asthma management during,
801
for biliary atresia,
1387
for breast alterations,
e545-4
for coccidioidomycosis,
1068
for congenital diaphragmatic hernia,
596,
596f
for congenital heart disease,
1602-1610,
1605t
coarctation of the aorta,
1569
postoperative management following,
1603-1604
ventricular septal defect,
1558
contraceptive, special needs girls and,
1875
diabetes mellitus management during,
1987,
1987t
for gastroesophageal reflux disease,
1268-1269
for Graves disease,
1912t
for intestinal malrotation,
1281
for neonatal necrotizing enterocolitis,
603
for nontuberculous mycobacterial lymphadenitis,
1015
for peptic ulcer disease,
1294
for pyloric stenosis,
1275
for septic arthritis,
2400
for ulcerative colitis,
1300
Surgical otoscope head,
2202
Surrogate endpoints in pharmacodynamics,
e57-9
Survival Epidemiology and End Results (SEER),
1727f
Susceptibility testing, antimicrobial,
e164-3
in nontuberculous mycobacteria,
1015
Suspending fluids in immunizing agents,
883
Sustained attention,
e29-3
Sutures
cranial
in neurologic examination,
e584-2
for laceration closure,
341
Swallowed blood syndrome,
621
Swallowing studies in aspiration syndromes,
1472t
Sweat glands
cystic fibrosis and,
1487
Swimming pool granuloma,
1013
Swyer-James syndrome,
1461
Sylvian aqueduct syndrome,
2161
Symbols in laboratory testing,
e708-1t
Symmetric progressive erythrokeratoderma,
2270-2271
Symptomatic seizure,
2013
Symptom review in psychiatric diagnostic evaluation,
58
Synapses, development and,
e6-1
Synchronized cardioversion,
288-289
Syndrome of inappropriate antidiuretic hormone (SIADH)
diagnostic criteria for,
217t
plasma osmolality and,
e52-4
Synovial fluid analysis in septic arthritis,
2399
Syntax difficulties,
e29-2
Syphilis,
1016-1023
cerebrospinal fluid findings in,
2088t
clinical manifestations and laboratory findings in,
1016-1018
in immigrant children,
133
maternal
fetal and neonatal effects of,
e89-3t
oral ulcerations in,
1260t
Systematic desensitization for phobias,
81
Systemic lupus erythematosus (SLE),
841-846
alveolar hemorrhage with,
1499
cerebrospinal fluid findings in,
2088t
clinical manifestations of,
843,
843t
fever of unknown origin in,
899
glomerulonephritis associated with,
1788-1789
insulin receptors autoantibody development in,
1996
myocardial disease with,
1629t
oral ulceration in,
1260t
Systemic vascular resistance in shock,
311t
System of care, planning and implementing
Systems approach in patient safety,
e2-6
Systolic ejection murmur, auscultation of,
1535
Systolic overload pattern,
1539
T
Tachycardia
in acute intermittent porphyrias,
e85-6
in
Corynebacterium diphtheriae-associated toxic cardiomyopathy,
e180-2
sinus,
1616t
supraventricular tachycardia
versus,
1613
Tachypnea
in acutely ill child,
275
maintenance water and electrolytes and,
244
as manifestation of extrapulmonary disease,
1526
transient of newborn,
590
respiratory distress syndrome
versus,
583-584
Tacrolimus
diabetes associated with,
1997
for nephrotic syndrome,
1805
Tandem mass spectrometry (MS/MS),
e707-2
Tardive dyskinesia, drug-induced,
2059
Targeted array comparative genomic hybridization (aCGH),
398
Target sign in aspergillosis,
1060
Taussig-Bing malformation,
1582
Taxus species toxicity,
269t
Tazarotene for acne,
2325t
Tazobactam/piperacillin,
645t
T cells,
722
abnormalities of
inheritance in development of,
e117-6
in adverse drug reactions,
824
in atopic dermatitis,
802
in juvenile idiopathic arthritis,
831,
831f
in systemic lupus erythematosus,
843
T cell antibodies in renal transplantation,
e530-3
T cell receptor-CD3 complex (Ti-CD3)
T cell receptor recombination excision circles (TRECs),
e117-1-e117-2
Teamwork for patient safety,
e2-6
Technology, health information,
e2-7
Tedinopathy, as sports injury,
2407
Teeth
congenital erythropoietic porphyria effects on,
e85-9,
e85-9f
disorders of
associated with other conditions,
1251,
1251t
effects of eating disorders on,
93t
effects of malnutrition on,
175t
during middle childhood,
36
Teething,
1257
home remedies among African Americans for,
e4-2t
Telangiectasia
hereditary hemorrhagic,
2230
Telangiectasia macularis eruptiva perstans,
2281
Telangiectatic osteosarcoma,
1763
Telomerase in oncogenesis,
e486-4
Temperature
Celsius and Fahrenheit equivalents,
e708-16t
maintenance of
for low birthweight infant,
559
Temperature receptors in respiration regulation,
1421
Temporal bone
otitis media complications within,
2210
Temporomandibular joint (TMJ) disease,
832,
834f
Tendon reflexes
in hypoxic-ischemic encephalopathy,
571t
in neuromuscular disorders,
2109
Tenosynovitis-dermatitis syndrome, gonococcal,
937
Tention-type headache (TTH),
2046
Teratoid/rhabdoid tumor,
1752
Terazosin for systemic hypertension,
1645t
Terbinafine for tinea capitis,
2311
Testes
defects in differentiation of,
1962
embryonic regression syndrome of,
1963
newborn assessment of,
536
pseudoprecocity resulting from tumors of,
1943-1950
Testicular adrenal rests,
e578-1
Testicular dysgenesis syndrome,
1945
Testicular feminization syndrome,
1365
Testicular regression syndrome,
1944
Testosterone
in ovarian carcinomas,
1872t
in testicular function,
e576-1
Testosterone precursors for performance enhancement,
2423
Tetanus and diphtheria toxoid (Td),
884t
Tetanus immunoglobulin (TIG),
882t,
992
Tetanus toxoid, reduced diphtheria toxoid and acellular pertussis (Tdap) vaccine,
884t,
948,
993
recommended schedule for,
888f
Tetany
in pseudohypoparathyroidism,
1919
Tetracaine, epinephrine, and cocaine (TAC),
367-368
Tetracycline,
e173-13
discolored teeth due to,
1251
for louse-borne typhus,
1048
possible adverse reactions to in premature infant,
563t
for Rocky Mountain spotted fever,
1043
Tetrahydrobiopterin (BH
4) deficiency,
446
“Tet spells” in tetralogy of Fallot,
1574
Textiles, infection protection and control and,
e166-2t
TG2 in celiac disease,
1308
Thalassemia(s),
1674-1677
hematopoietic stem cell transplantation for,
759,
760f
Thalidomide
for actinic prurigo,
2257
Theophylline
for allergic disease,
772
Thermodilution measurement of cardiac output,
1547-1548
Thiamine-responsive maple syrup urine disease,
431
Thiamine-responsiveness megaloblastic anemia (TRMA),
191,
e448-5
Thiazide diuretics
for hypertension of chronic kidney disease,
1825
metabolic alkalosis due to,
236
Thin basement membrane disease (TBMD),
1783
Thiopental
for status epilepticus,
2039t
Thioridazine toxicity,
251t
Third-degree heart block,
1618
Third heart sound, auscultation of,
1533
Thirst, regulation of,
1882
Thoracic dystrophy, asphyxiating,
2434
Thoracic-pelvic-phalangeal dystrophy,
1517
Thoracoscopic surgery, video-assisted
Three-dimensional echocardiography,
1543,
1544f
317 Discretionary Federal Grant Program,
885
3D reconstruction of computed tomography,
1546,
1547f
Thrills,
1533
in tetralogy of Fallot,
1574
Throat culture,
e164-2
in group A streptococci infection,
917
Thrombocytopenia,
1714
due to acquired disorders causing decreased production,
1721
due to ehrlichiosis,
1049
hematuria associated with,
1796
in hemolytic-uremic syndrome,
1793
immunodeficiency with eczema and,
734-735
in Rocky Mountain spotted fever,
1042
Thrombocytopenia-absent radius (TAR) syndrome,
1531t,
1719
Thrombocytosis in pertussis,
945
Thromboembolism, venous,
1709
Thrombosis
cerebral, with tetralogy of Fallot,
1576
deep vein,
1709
estrogen contraceptives and,
1875
due to exchange transfusion,
618
renal transplantation and,
e530-2
renal vein,
1709
in newborn assessment,
535
Thrombotic predisposition, testing for,
1699
Thrombotic thrombocytopenic purpura (TTP),
1718-1719
Thumb method of chest compressions,
291,
292f
Thunderclap headache,
2084
Thymectomy for myasthenia gravis,
2135
Thymidine kinase in congenital dyserythropoietic anemia,
e446-1t
Thymidine kinase 2 (TK2),
1406
Thymidine phosphorylase deficiency,
e83-9
Thymoglobulin in renal transplantation,
e530-3
Thyroglobulin,
e557-1
reference values for,
1899t
synthesis defects of,
1896
Thyroglossal cysts and sinuses,
2221
Thyroid antiperoxidase antibodies
in lymphocytic thyroiditis,
1903
Thyroid function tests,
1899t
Thyroid gland
development and physiology of,
e557-1
disorders of
thyroxine-binding globulin defects as,
e558-1
transport defects and,
1896
Thyroid-related ophthalmopathy,
2182
Thyroid-stimulating hormone (TSH),
e550-1
in intellectual disability,
127t
in thyroid hormone unresponsiveness,
1897
Thyrotoxicosis, myopathies due to,
2129
Thyrotoxic periodic paralysis,
222-223
Thyrotropin
unresponsiveness of,
1897
Thyrotropin receptor-blocking antibody,
1896
Thyrotropin receptor-stimulating antibody (TRSAb)
in congenital hypothyroidism,
1913
Thyrotropin-releasing receptor abnormalities,
1897
Thyroxine-binding globulin (TBG)
Thyroxine (T
4),
1894,
e557-1
in congenital hypothyroidism,
1899
defective synthesis of,
1896
testing of,
e557-1
in intellectual disability,
127t
in thyroid hormone unresponsiveness,
1897
Thyroxine (T
4) binding globulin in congenital hypothyroidism,
1899
Tiagabine
adverse effects of,
2031t
Tibia
congenital and angular deformities of,
2350-2351
normal development of,
2344
Tibial longitudinal deficiency,
2351
Tic disorders,
76
group A streptococci infection and,
919
Tick, removal of attached,
1043
Tick-borne encephalitis (TBE),
1146
Tick-borne illness
hemorrhagic fevers,
1150t
Mediterranean spotted fever,
1044
Timeliness in quality of care,
e2-1
Tinea in child-care setting,
e167-1t
Tinea nigra palmaris,
2313
Tissue analysis, fetal,
543t
Tissue culture cytotoxicity assay,
995
Tissue factor in hemostasis,
1694
Tissue hypoxia, respiratory alkalosis due to,
240,
241t
Tissue plasminogen activator (TPA)
reference values for,
1698t
T-lymphocyte-dependent vaccine,
883
Tobacco smoke, exposure to,
e700-2
Tocilizumab for rheumatic disease,
e148-6
Toddler
behavioral and psychosocial assessment of,
56
child restraint in motor vehicles for,
21t
disruptive behavioral disturbances in,
99
drowning or submersion injury to,
342
growth and development of,
31-33
injury risk factors for,
20
intellectual disability in,
125t
leading causes of death for,
5t
lower extremity fracture of,
2392
response to death of,
e16-3
Toll-like receptors (TLRs),
855
Tolterodine for nocturnal incontinence,
1852
Tomaculous neuropathy,
2140
Tomography, positron emission,
e584-11
Tone, muscle
in neuromuscular disorders,
2109
Tongue
oral hairy leukoplakia of,
2299
strawberry in Kawasaki disease,
863,
864f
Tonic clonic reflex in neurologic examination,
e584-7
Tonsillectomy
for recurrent pharyngitis,
1440
Topical therapy
for skin disorders
nonsteroidal antiinflammatory drugs,
2217
Topiramate
adverse effects of,
2031t
for weight loss in adults,
187t
Total body irradiation (TBI), late effects of,
e133-1
Total body water (TBW),
e52-1-e52-3
drug distribution and,
e57-5
hypervolemic hyponatremia and,
216
Total cholesterol, obesity and,
185t
Total hemolytic complement activity (CH
50),
753
Total parenteral nutrition (TPN)
cholestasis associated with,
e352-2
for premature and low birthweight infants,
559-560
Tourette’s syndrome (TS),
76-77
group A streptococci infection and,
919
Toxic shock syndrome toxin-1 (TSST-1),
904
Toxic shock syndrome (TSS)
Toxigenic
Corynebacterium diphtheriae,
e180-1
Toxin(s)
Clostridium difficile,
1313
erythrogenic in scarlet fever,
916
hemolytic anemia secondary to,
e459-1
in respiratory distress,
316
Trachea
compression of as oncologic emergency,
e488-6t
stenosis, webs, and atresia of,
1452
Tracheitis
Staphylococcus aureus in,
905
Tracheobronchitis, acute,
1459
Tracheostomy, home mechanical ventilation through,
332-333
Tracheotomy for infectious acute upper airway obstruction,
1448
Trafficking in children,
136
Training for emergencies,
e61-1
Transcatheter closure of patent ductus arteriosus,
1560f,
1561
Transcondylar fracture,
2392
Transcranial Doppler (TCD) assessment in sickle cell disease,
1667
Transcription-mediated amplification (TMA),
1036
Transcutaneous electrical nerve stimulation (TENS),
371
Transdermal fentanyl patch for pain management,
155t-156t
Transferrin
in malnutrition with chronic diarrhea,
1343t
Transferrin receptors in iron deficiency-anemia,
1657t
Transforming growth factor-β (TGF-β)
Marfan syndrome and,
2440
neutralizing antibodies,
2445
Transglutaminase deficiency,
1704
Transient hyperammonemia of newborn,
452-453
Transient lower esophageal sphincter relaxation (TLESR),
e310-1
gastroesophageal reflux disease and,
1266
Transient monoarticular synovitis of hip,
2360
Transient neonatal diabetes mellitus (TNDM),
1995
Transient synovitis of hip,
2413
Transient tachypnea of newborn (TTN),
590
Transillumination
in acute inguinal-scrotal swelling,
1364-1365
Transitional object,
31-32
Transjugular intrahepatic portosystemic shunt (TIPS),
e359-3
Transmembrane receptors, skeletal dysplasias involving,
2428-2430
Transmission disequilibrium test (TDT),
e77-3
Transplacental chemical exposure,
e700-3
Transplacental hemorrhage, anemia due to,
612-613
Transplantation
candidal infection associated with,
1055
for genetic disorders,
380
Transport
of chronically ill child,
e39-3
communications and dispatch center in,
e61-7
educational outreach in,
e61-9
effects on physiology,
e61-8
of folate, congenital abnormalities of in anemia,
e448-1
ground
versus air ambulance for,
e61-8
medical control physician in,
e61-7
of vitamin B
12, congenital abnormalities of in anemia,
e448-4
Transporters
ion, skeletal dysplasias involving,
2430-2431
Transposition of the great arteries (TGA)
with ventricular septal defect,
1587
Transtubular potassium gradient (TTKG),
221
Traumatic brain injury (TBI),
297-301,
298f-301f
attention deficit/hyperactivity disorder following,
108
Traumatic intracranial hemorrhage in newborn,
566
Travel
underlying medical illness and,
e168-1
Trazodone
for depression and anxiety symptoms,
63t
for sleep disturbance/insomnia in palliative care,
155t-156t
Treacher Collins syndrome
congenital heart disease with,
1531t
oral manifestations of,
1254
Treatment, religious objections to,
e3-3-e3-4
Treatment plan in psychiatric diagnostic evaluation,
60
Treponema pallidum hemagglutination assay (TPHA),
1019-1020
Treponema pallidum particle agglutination test (TPPA),
1019-1020
Treprostinil for pulmonary hypertension,
1602t
Triage
in international pediatric emergency medicine,
e61-15
Triage officer model for emergency care,
e61-12
Triamterene for systemic hypertension,
1645t
Triatomines in trypanosomiasis,
1195
Trichloroacetic acid for genital warts,
713t
Trichloroethylene, as inhalant,
681t
Trichloroethylene exposure,
e700-1t
Tricho-hepato-enteric (THE) syndrome,
1311-1312
Trichopoliodystrophy,
2292
Trichorrhexis invaginata,
2293
Tricuspid regurgitation,
1572
Tricuspid valve disease,
1628
Tricyclic antidepressants (TCAs)
for attention deficit/hyperactivity disorder,
111t
for depression and anxiety symptoms,
63t
for neuropathic pain,
368t
in psychopharmacology,
62
Trientine for Wilson disease,
1392
Trifunctional protein (TFP), mitochondrial deficiency,
460
Trigger thumb and fingers,
2387
Triglycerides,
479t
laboratory testing of in obesity,
185t
Triiodothyronine (T
3),
1894,
e557-1
in congenital hypothyroidism,
1899
in thyroid hormone unresponsiveness,
1897
Triiodothyronine (T
3) resin uptake test,
1899t
Trimethoprim-sulfamethoxazole (TMP-SMX),
e173-3,
e173-4t-e173-11t
for cystic fibrosis lung infection,
1492t
for diarrheagenic
Escherichia coli,
964-965
for infectious diarrhea,
1337t
for
Paracoccidioides brasiliensis,
e233-1
for
Shigella infection,
961
for
Staphylococcus aureus,
907t
for
Toxoplasmosis gondii prophylaxis in HIV infection,
1168t-1171t
for vulvovaginitis,
1868t
Triose phosphate isomerase (TPI) deficiency,
1677
Trisomy 9,
404t
congenital heart disease with,
1531t
Trisomy 12p,
404t
congenital heart disease with,
1531t
Trisomy by trisomy rescue,
413
Trochlear nerve
neurologic examination of,
e584-4
Tropheryma whipplei,
1314
in infective endocarditis,
1624t
Trophic feeding of premature infant,
561
Tropical pancreatitis,
1373
Tropical splenomegaly syndrome,
1206
Truncal ataxia in neurologic examination,
e584-7
Trypsinogen
serum in exocrine pancreatic function,
1307
Tsetse fly, in trypanosomiasis,
1190
Tsutsugamushi fever,
1045
Tube feeding in infant botulism,
990
Tuberculin skin testing (TST),
1001,
1002t
in fever of unknown origin,
902
of immigrant children,
133
Tuberculosis (TB),
996-1011,
996f-997f
abdominal and gastrointestinal,
1006
exclusion from day care due to,
e15-2t
in immigrant children,
133
inflammatory bowel disease
versus,
1298t
lymphohematogenous (disseminated),
1004
respiratory culture in,
e164-2
Tuberculosis verrucosa cutis,
2307
Tuberculous adrenalitis,
1925t
Tubes
chest, for emergencies,
295
endotracheal
manual ventilation before and after,
320-321
medications for placement of,
321t
for respiratory distress and failure,
320
size and depth dimensions for,
320t
Tubular proteinuria,
1801
Tubules, renal
disorders of
Gitelman syndrome as,
1814
nephrogenic diabetes insipidus as,
1812
renal tubular acidosis as,
1811f
Tubulointerstitial fibrosis,
e502-4
Tumor(s)
See also Malignancy
specific types
desmoplastic small round cell,
1773
gonadotropin-secreting, precocious puberty due to,
1891
hepatic, precocious puberty due to,
1891
incidence and survival rates for,
1726t
neural crest, congenital central hypoventilation syndrome with,
1520-1521
Tumor necrosis factor α (TNF-α)
in Rocky Mountain spotted fever,
1041
in sudden infant death syndrome,
1427
Tumor necrosis factor α (TNF-α) antagonists
for juvenile idiopathic arthritis,
838t
for spondyloarthritides,
e150-2
Tumor necrosis factor receptor-associated periodic syndrome (TRAPS),
855t,
858,
859f
Tumor suppressor genes, alterations in regulation of,
e486-1
T2-weighted magnetic resonance imaging in sickle cell disease,
1666-1667,
1666f
21st century, information explosion of,
11-12
Twenty-four hour electrocardiography (Holter) recordings,
1614-1615
Twin reversed arterial perfusion (TRAP) syndrome,
554
Twins
monozygotic
versus dizygotic,
553-554
Twin-twin transfusion syndrome,
554
TWIST heterogenous,
2012t
“Two-hit” model of cancer development,
e486-1
22q11.2 deletion syndrome,
2382,
2382f
congenital heart disease and,
e418-1
Tylophora indica for asthma,
271t
Tympanic membrane (TM)
cholesterol granuloma of,
2212
in otitis media with effusion,
2204f
traumatic perforation of,
e634-1
Type 1 diabetes mellitus (T1DM),
1969-1990
anxiety and depression in,
1986
behavioral/psychologic aspects of,
1986
catabolic losses in,
1980
clinical manifestations of,
1975
cognitive function and,
1986
dental problems associated with,
1251t
fear of self-injecting and self-testing in,
1986
hypothyroidism with,
1901
metabolic acidosis in,
232
nonketotic hyperosmolar coma in,
1981
pancreas and islet transplantation and regeneration for,
1989-1990
treatment of,
1976-1986
amylin based adjunct therapy for,
1979
glycemic control in,
1984
of new-onset diabetes without ketoacidosis,
1976
real-time continuous glucose monitoring in,
1983-1984
Type 2 diabetes mellitus (T2DM),
1990-1993
environmental and lifestyle-related risk factors in,
1991
epigenetics and fetal programming in,
1991
Type I collagen, defects in,
2437
Type III secretion system (TTSS-3),
Shigella,
959
Type II secretion system (TTSS-1),
Salmonella,
950
Typhoid fever,
954-958
differential diagnosis of,
957
Tyrosine hydroxylase deficiency,
445
Tyrosinemia
transient of newborn,
423
Tzanck smear,
e637-2
in varicella-zoster virus infection,
1108
V
Vaccine Adverse Event Reporting System (VAERS),
885
Vaccine-associated paralytic poliomyelitis (VAPP),
1082,
1084
Vaccine encephalopathy, febrile seizures with,
2017
Vaccine(s),
883-884,
884t
adverse reactions to,
827
chronic kidney disease and,
1825
congenital heart disease and,
1603
group B streptococcus,
928
Haemophilus influenzae type B,
943
for homosexual youth,
659
immigrant children and,
132,
134
international practices on,
893-895
pneumococcus,
884t,
2095
pneumonia hospitalization and,
1479
precautions and contraindications for,
892-893
respiratory syncytial virus,
1129
sudden infant death syndrome and,
1425
T lymphocyte-dependent,
883
type 1 diabetes mellitus and,
1972
websites and resources associated with,
894t
Vaccine Safety Datalink (VSD),
886
Vaccines for Children (VFC) program,
885
Vaccinia immune globulin,
882t
Vagal nerve stimulation for seizures,
2032-2033
Vagina
traumatic injury to, vaginal bleeding due to,
1869
Vaginal contraceptive ring,
697
special needs girls and,
1875
Vaginal orifice, neonatal examination of,
e542-1
Vaginitis,
708,
1865
group A streptococcus in,
917
Vaginosis, bacterial
prophylaxis following rape,
704t
Vagus nerve, neurologic examination of,
e584-5
Valeriana officinalis for sedation,
271t
Valerian for sedation,
271t
Validity
in quality measurement,
e2-2t
Valine, defects in metabolism of,
430-438
Valproate
for neuropathic pain,
368t
for status epilepticus,
2039t
Valproic acid
adverse effects of,
2031t
for Landau-Kleffner syndrome,
2024
Valvular heart disease
See also specific valves
due to acute rheumatic fever,
922
Valvuloplasty
balloon
for aortic stenosis,
1566
for pulmonary valve stenosis,
1563
Vancomycin,
e173-3,
e173-4t-e173-11t
for
Clostridium difficile infection,
995
for cystic fibrosis lung infection,
1492t
for infective endocarditis,
1625t
for meningococcal disease,
932
for pneumococcal meningitis,
913
Van den Bergh reaction,
603
Vanishing twin syndrome,
553
Variant surface glycoproteins (VSG),
1191
Variceal hemorrhage,
1376
Varicella-zoster virus immune globulin (VariZIG),
882t,
1110,
e237-5
for neonatal varicella,
1106
Varicella-zoster virus (VZV),
1104-1110,
1105f,
1107f,
1109t
exclusion from day care due to,
e15-2t
immunofluorescent-antibody testing of,
e164-3
maternal
fetal and neonatal effects of,
e89-3t
poliovirus infection
versus,
1085t
in viral meningoencephalitis,
2096
Vascular compartment, pulmonary edema and,
1468
Vascular endothelial growth factor (VEGF)
in ovarian carcinomas,
1872t
in retinopathy of prematurity,
2174
in sudden infant death syndrome,
1422,
1427
Vascular events, seizures due to,
2034
Vasculitis
hypocomplementemic urticarial,
876
leukocytoclastic,
876
due to cat-scratch disease,
985
renal, nephrotoxins in,
1817t
small vessel, with hepatitis C,
1401
Vasculitis syndromes,
867-876,
868t,
876t
antineutrophil cytoplasmic antibodies (ANCA)-associated vasculitis as,
874-876
cutaneous manifestations of,
e637-5
polyarteritis nodosa and cutaneous polyarteritis nodosa as,
872-874,
873f
Vas deferens injury, related to inguinal hernia repair,
1368
Vasoactive intestinal polypeptide (VIP),
e333-2t
Vasodilators
for systemic hypertension,
1645t
Vasopressin-resistant diabetes insipidus,
1882
VATER syndrome,
1262
congenital heart disease with,
1531t
VEGFR-1, 2, cancer therapy specific to,
e488-2t
Vein of Galen malformation,
1639
Velopharyngeal dysfunction (VPD),
1253
Venereal Disease Research Laboratory (VDRL) test,
1019,
1019f,
1021
Venezuelan equine encephalitis (VEE),
1144-1147
Venlafaxine
for depression and anxiety symptoms,
63t
Venography
computed tomography, in cerebral sinovenous thrombosis,
2083,
2083f
magnetic resonance, in neurologic examination,
e584-11
Veno-occlusive disease (VOD), of liver,
e352-3
Venous patterns, assessment in neurologic examination,
e584-2
Venous thrombosis, renal transplantation and,
e530-2
Ventilation
insufficiency of, due to paralytic poliomyelitis,
1084,
1086
manual
in preintubation and postintubation periods,
320-321
partial liquid, for congenital diaphragmatic hernia,
596
Ventilation deficit assessment in respiratory distress and failure,
318-319
Ventilation index (VI),
319
Ventilation-perfusion (V/Q) mismatch,
317-318
Ventilation-perfusion (V/Q) radionuclide scan,
1502
Ventilator dependence,
PHOX2B gene and,
1520
Ventilatory failure, hypothyroidism-associated,
1903t
Ventilatory support in congenital central hypoventilation syndrome,
1522
Ventricle
double-outlet right,
1582
with malposition of great arteries,
1588-1589
with pulmonary stenosis,
1588
embryonic development of,
1527
in fetal circulation,
1529
in transitional circulation,
1529
Ventricular accelerated rhythm,
1616
Ventricular assist device (VAD),
314
Ventricular fibrillation,
1616
Ventricular hypertrophy
radiographic assessment of,
1537
systemic hypertension with,
1642
Ventricular inversion,
1595
Ventricular septal aneurysm,
1557
Ventricular septal defect (VSD),
1556-1558,
1556f-1557f
coarctation of the aorta,
1570
embryonic development of,
1527
supracristal, with aortic insufficiency,
1559
transitional circulation and,
e418-1
transposition of the great arteries,
1587
with transposition of the great arteries and pulmonary stenosis,
1574,
1583f
Ventriculography in tetralogy of Fallot,
1575,
1575f
Verbal auditory agnosia,
119
Vericonazole for blastomycosis,
1065
Vermont Oxford Network (VON),
e2-4
Vernal keratoconjunctivitis,
810,
810f
Verotoxin in hemolytic-uremic syndrome,
1791-1792
Versenate for lead poisoning,
2453
Vertebral apophysis, slipped,
2377
Vertigo
in neurologic examination,
e584-4
Very long chain acyl CoA dehydrogenase (VLCAD) deficiency,
457t,
460
Very long chain fatty acids (VLCFA) disorders,
462-470
adrenoleukodystrophy (X-linked) as,
467-470
Vesicle, examination of,
2215
Vesicular hand and foot dermatitis,
2253,
2253f
Vestibulocochlear nerve, neurologic examination of,
e584-5
Vestibulopathy, strokelike events
versus,
2086
Video-assisted thoracoscopic surgery (VATS)
Videofluoroscopic swallow study (VSS),
1472t
Vigabatrin
adverse effects of,
2031t
Vinblastine for cancer therapy,
e488-4t
Vineland Adaptive Behavior Scale (VABS),
127
Viral infections
arthritis associated with,
840,
840t
dengue fever and dengue hemorrhagic fever as,
1147-1150
fever of unknown origin in,
900t
human herpesviruses 8,
1121
in meningoencephalitis,
2095-2097
cerebrospinal fluid findings in,
2088t
predisposition to due to immunodeficiency,
716t
stem cell transplantation and,
e171-1
traveler’s diarrhea due to,
1338t
in type 1 diabetes mellitus development,
1971
Viral load in HIV infection,
1161
Viremia, herpes simplex virus,
1099
Virologic assay for hepatitis C virus,
1401
Visceroatrial situs,
1595
Viscum album, potential toxicity of,
272t-273t
Vision
Neonatal Intensive Care Unit Neurobehavioral Scale and,
624t
testing of,
2149t
in intellectual disability,
127t
in neurologic examination,
e584-4
Visual acuity,
2148
assessment in neurologic examination,
e584-3
during preschool years,
33
in vision screening,
2149t
Visual analog pain scales (VAS),
361,
363t
Visual reinforcement audiometry (VRA),
2194
Vital signs in pediatric emergency assessment,
279,
280t
Vitamins
for premature and low birthweight infants,
562
supplemental
for chronic diarrhea,
1345
nutritional aspects of,
169
Vitamin A
absorption, transport, metabolism, and storage of,
188
function and mechanism of action of,
189
supplementation,
190
for neonatal cholestasis,
1387
for respiratory distress syndrome,
586
Vitamin B
6-dependent epilepsy,
453-455
Vitamin B
6 dependence syndrome,
196
Vitamin C,
194t,
198
dietary needs and sources of,
198
for premature and low birthweight infants,
560
Vitamin D,
e41-16-e41-17
deficiency of
calcium deficiency and,
206
due to chronic renal failure,
205-206
due to malabsorption,
1318
physical and metabolic properties and food sources of,
201t
supplementation,
165
for premature and low birthweight infants,
560
Vitamin D-dependent rickets
dental problems associated with,
1251t
Vitamin E
deficiency of,
e49-1-e49-2
ataxia with isolated,
e49-1
clinical manifestations of,
e49-1
diagnosis and differential diagnosis of,
e49-1
laboratory findings in,
e49-1
myopathy associated with,
2132
physical and metabolic properties and food sources of,
201t
for premature and low birthweight infants,
560
possible adverse reactions to,
563t
supplementary for neonatal cholestasis,
1387-1388
Vitamin K,
e41-17
injection of in newborn,
537
physical and metabolic properties and food sources of,
201t
possible adverse reactions to in premature infant,
563t
Vitamin K-deficiency bleeding (VKDB),
210
Vitamin K-dependent factors, deficiency of,
620-621
Vitelliform degeneration, Best,
2178
Vitreoretinopathy, familial exudative,
2179
Vocal cord dysfunction (VCD), asthma
versus,
783
Vocal cord paralysis,
1451
Vogt-Koyanagi-Harada syndrome,
2240
Vohwinkel palmoplantar keratoderma,
2273
Voiding cystourethrogram (VCUG)
in urinary tract obstruction,
1840
Voiding dysfunction,
1847-1852
diurnal incontinence in,
73
infrequent voiding as,
1850
without incontinence,
1851
Volatile substance abuse (VSA),
681-682
Volleyball, injuries in,
e684-2
Volume of distribution,
e57-3
Volume support ventilation (VSV),
325
Vomiting,
1242-1243
in acutely ill child,
275
differential diagnosis of,
1242t
exclusion from day care due to,
e15-2t
habits regarding in eating disorders,
92t
Jamaican vomiting syndrome,
529
nondigestive causes of,
1241t
in pyloric stenosis,
1274
therapy for
nonpharmacologic and supportive,
1245t
von Hippel-Lindau disease (VHL),
2052
brain tumors associated with,
1747t
cardiac manifestations of,
1531t
von Recklinghausen disease,
2237
von Willebrand factor
reference values for,
1698t
Vorner palmoplantar keratodermas,
2273f
VPS33B gene defect,
1383t
Vulva
neoplasm of,
1873
vaginal bleeding due to,
1869
traumatic injury to, vaginal bleeding due to,
1869
VX-770 for cystic fibrosis,
1493