cryptococcus table classification dosing severity coding pathophysiology classes algorithm 21ohd

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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 ... Severity depends ... #21HydroxylaseDeficiency #21OHD ... #pathophysiology

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