Pediatrics peds syndrome symptoms cardiology physicalexam congenital constipation pathophysiology 21ohd schematic

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21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings
Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase

also known as "congenital ... Signs/Symptoms/Complications ... #pathophysiology ... endocrinology #peds ... #pediatrics

Fontan Procedure Schematic
A Fontan is done in most children (approximately 90%) who effectively have a single

Fontan Procedure Schematic ... syndrome. ... #Diagram #congenital ... #Cardiology #Peds ... #Pediatrics #Pathophysiology

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