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
Hypokalemia Evaluation Algorithm

Before evaluating hypokalemia, life threatening complications such as arrhythmias and paralysis should be looked
Algorithm Before ... treated with IV potassium ... urinary losses: • High ... Metabolic Alkalosis: Emesis ... #differential #
Pediatric Vomiting - Gastrointestinal and Systemic Causes - Differential Diagnosis Algorithm
Hepatobiliary:
 • Acute Hepatitis
 • Acute
Pediatric Vomiting ... - Differential ... • Uremia • Hypercalcemia ... Psychogenic #Emesis ... #Causes #Peds #