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peds 21hydroxylasedeficiency cardiology diagram endocrinology fontan genetics procedure schematic
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
also known as "congenital ... , vomiting • Late ... #21HydroxylaseDeficiency #21OHD ... #pathophysiology ... endocrinology #peds #pediatrics
Fontan Procedure Schematic A Fontan is done in most children (approximately 90%) who effectively have a single
valvular atresia or a congenital ... flow into the pulmonary ... Schematic #Diagram #congenital ... Cardiology #Peds #Pediatrics ... #Pathophysiology
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