Photo skin pediatrics causes algorithm infant acute abdominalpain clinical 21ohd patterns

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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 ... deficiencies present in infants ... cold & mottled skin ... #21HydroxylaseDeficiency #21OHD

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