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21hydroxylasedeficiency cirrhosis endocrinology findings genetics hepatology liverfailure signs
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
Signs/Symptoms/Complications ... Hyperkalemia, Hypoglycemia ... #pathophysiology ... endocrinology #peds ... #pediatrics
Clinical features of Liver Disease in Children #Cirrhosis #LiverFailure #Signs #Symptoms #PhysicalExam #Findings #Diagnosis #Peds #Pediatrics #Hepatology **
Clinical features ... LiverFailure #Signs #Symptoms ... #PhysicalExam # ... Findings #Diagnosis ... #Peds #Pediatrics
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