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21hydroxylasedeficiency 21ohd anatomy diagram endocrinology fetal fontan procedure schematic
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
enzyme 21-OHase causes ... also known as "congenital ... #21HydroxylaseDeficiency #21OHD #pathophysiology ... #genetics #endocrinology ... #peds #pediatrics
Fetal and Post Transition Circulation In the fetal circulatory system, oxygenated blood is delivered via the umbilical
Post Transition Circulation ... oxygenated blood passes ... #Pathophysiology ... #Cardiology #Anatomy ... #Peds #Pediatrics
Fontan Procedure Schematic A Fontan is done in most children (approximately 90%) who effectively have a single
valvular atresia or a congenital ... pulmonary and systemic circulation ... Schematic #Diagram #congenital ... #Cardiology #Peds ... #Pediatrics #Pathophysiology
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