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pediatrics peds 21hydroxylasedeficiency diagnosis differential emesis endocrinology genetics vomiting
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
enzyme 21-OHase causes ... deficiencies present in infants ... Signs/Symptoms/Complications ... #21HydroxylaseDeficiency #21OHD ... #pathophysiology
Pediatric Vomiting - Gastrointestinal and Systemic Causes - Differential Diagnosis Algorithm Hepatobiliary: • Acute Hepatitis • Acute
Differential Diagnosis Algorithm ... • Small/Large Bowel ... Head Trauma • Brain ... #Causes #Peds # ... Pediatrics
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