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21hydroxylasedeficiency 21ohd diagnosis endocrinology genetics pathophysiology tetralogy
Tetralogy of Fallot 1. Right ventricular outflow tract obstruction 2. Right ventricular hypertrophy 3. Ventricular septal
Tetralogy of Fallot ... #Tetralogy #Fallot ... #Peds #Pediatrics ... #Cardiology #Signs ... #Symptoms #Diagnosis
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
enzyme 21-OHase causes ... Signs/Symptoms/Complications ... vomiting • Late (shock ... endocrinology #peds ... #pediatrics
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