ScarletFever trunk pediatrics pathophysiology congenital 21ohd 21hydroxylasedeficiency - GrepMed

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

also known as "congenital ... a scrotum #21HydroxylaseDeficiency ... #21OHD #pathophysiology ... endocrinology #peds #pediatrics

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