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peds 21hydroxylasedeficiency cardiology 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 ... #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 ... Procedure #Schematic #Diagram ... #congenital #Cardiology ... #Peds #Pediatrics ... #Pathophysiology
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