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diagnosis 21hydroxylasedeficiency age cardiomyopathy endocrinology fontan hypertension management peripartum 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 ... #pathophysiology ... #genetics #endocrinology ... #peds #pediatrics
Age Distribution of Hypertension Etiologies < 1 month - Renal arterial thrombosis - Congenital renal disease -
thrombosis - Congenital ... #Hypertension #Causes ... #differential # ... age #pediatrics ... #peds
Fontan Procedure Schematic A Fontan is done in most children (approximately 90%) who effectively have a single
ventricle, either secondary ... Procedure #Schematic #Diagram ... #congenital #Cardiology ... #Peds #Pediatrics ... #Pathophysiology
Peripartum Cardiomyopathy - Summary 1. Definition • Towards the end of pregnancy to 5 months postpartum
exclude other causes ... Differential Diagnosis ... heart disease • Congenital ... Genetic predisposition ... #treatment
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