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peds endocrinology genetics 21hydroxylasedeficiency algorithm cah cardiology causes comparison congenitaladrenalhyperplasia diagnosis diagram fontan praderwilli procedure schematic syndrome treatment
Infographic depicting the main pearls of various types of congenital adrenal hyperplasia for the medical student.
various types of congenital ... adrenal hyperplasia ... algorithm #causes #pediatrics ... Endocrinology #Adrenal ... #pathophysiology
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
21-OHD in the adrenal ... also known as "congenital ... #21HydroxylaseDeficiency #21OHD ... #pathophysiology ... endocrinology #peds #pediatrics
Prader-Willi Syndrome: Pathogenesis and clinical findings • Maternal uniparental disomy: inheriting 2 copies of maternal chromosome
Poor suckling -> Neonatal ... sleep apnea, cor pulmonale ... Syndrome #genetics #pathophysiology ... #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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