Chart infant pediatrics table geriatrics pathophysiology comparison diabetes symptoms 21hydroxylasedeficiency 21ohd peds

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21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings
Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase

deficiencies present in infants ... Signs/Symptoms/Complications ... #21OHD #pathophysiology ... endocrinology #peds ... #pediatrics

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