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21hydroxylasedeficiency endocrinology genetics peds
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
Pathogenesis and Clinical ... enzyme 21-OHase causes ... cold & mottled skin ... #21HydroxylaseDeficiency #21OHD ... #pathophysiology
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