Apley sports algorithm peds causes clinical cardiology pediatrics congenital 21ohd - 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

Pathogenesis and Clinical ... enzyme 21-OHase causes ... also known as "congenital ... endocrinology #peds ... #pediatrics

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