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21hydroxylasedeficiency 21ohd diagnosis genetics
Croup Diagnosis and Management Pearls Common childhood illness, usually viral and self limiting. Characterised by a seal-like
and Management Pearls ... Commonly affects ... Symptoms usually ... #Diagnosis #Management ... #pediatrics #peds
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
Signs/Symptoms/Complications ... #21HydroxylaseDeficiency #21OHD #pathophysiology ... #genetics #endocrinology ... #peds #pediatrics
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