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21hydroxylasedeficiency endocrinology genetics pathophysiology pediatrics
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
mutation in CYP21A2 coding ... enzyme 21-OHase causes ... , vomiting • Late ... #21HydroxylaseDeficiency #21OHD ... endocrinology #peds
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