3 results
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings
Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
enzyme 21-OHase causes ... decr feeding, weight ... #21HydroxylaseDeficiency #21OHD ... endocrinology #peds ... #pediatrics
Causes of Pediatric Seizures - Differential Diagnosis Algorithm
Infantile:
 • Benign Focal Epilepsy of Infancy
 • West
Causes of Pediatric ... Seizures - Differential ... Diagnosis Algorithm ... #Causes #Peds # ... Pediatrics
Pediatric Vomiting - Gastrointestinal and Systemic Causes - Differential Diagnosis Algorithm
Hepatobiliary:
 • Acute Hepatitis
 • Acute
Pediatric Vomiting ... - Differential ... Diagnosis Algorithm ... • Uremia • Hypercalcemia ... #Causes #Peds #