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diagnosis algorithm causes childhood iem inbornerrors metabolism neonatology nicu table 21hydroxylasedeficiency 21ohd age cardiology developmentaldelay disorders endocrinology fallot hypertension immunization
Common Childhood Exanthems - Differential Diagnosis 1) Rubeola (Measles) - Measles morbillivirus (MeV) 2) Scarlet Fever - Streptococcus
Common Childhood Exanthems ... - Differential ... - Human Herpes Virus ... #Differential # ... Diagnosis #pediatrics
The six classic childhood exanthems • First Disease - Measles, Rubeola - Measles Virus • Second
classic childhood exanthems ... #childhood #exanthems ... #differential # ... diagnosis #peds ... #pediatrics
A schema of the pathophysiology of the inborn errors of metabolism, excluding complex storage diseases. Helps
schema of the pathophysiology ... MetabolicEmergency #Genetics ... #Pathophysiology ... Diagnosis #Algorithm #Differential ... #Neonatology #Peds
Lab patterns seen in Inborn Errors of Metabolism A table of lab values compiled from UpToDate and
from UpToDate and Pediatrics ... metabolicemergency-pathophysiology-differential-pediatrics-metabolism-algorithm-diagnosis ... #Neonatology #Peds ... #Pediatrics #Table ... #NICU #Genetics
Pediatric Mouth Disorders - Differential Diagnosis Algorithm Teeth: • Teething Painful - Gastrointestinal: • Crohn's Disease • Ulcerative
Pediatric Mouth ... Disorders - Differential ... Oral #Disorders #Differential ... Algorithm #Causes #Peds ... #Pediatrics
Tetralogy of Fallot Summary • Anatomy • Incidence • Pathophysiology • Presentation • Common Variants •
• Incidence • Pathophysiology ... • Associated Genetic ... management #cardiology #peds ... #pediatrics #treatment
Prader-Willi Syndrome: Pathogenesis and clinical findings • Maternal uniparental disomy: inheriting 2 copies of maternal chromosome
PraderWilli #Syndrome #genetics ... #pathophysiology ... #peds #pediatrics
Causes of Developmental Delay - Differential Diagnosis Algorithm Isolated Domain Delay - Reduced Respiratory Drive: • Cognitive
Developmental Delay - Differential ... Syndromic • Genetic ... DevelopmentalDelay #Differential ... Algorithm #Causes #Peds ... #Pediatrics
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
#21HydroxylaseDeficiency #21OHD #pathophysiology ... #genetics #endocrinology ... #peds #pediatrics
Acute Otitis Media: Pathogenesis and Clinical Findings (in Children) Upper Respiratory Tract Infection: - Bacterial: Streptococcus
Respiratory syncytial virus ... #OtitisMedia #pathophysiology ... symptoms #signs #peds ... #pediatrics
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