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pathophysiology 21ohd childhood endocrinology genetics immunization
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
enzyme 21-OHase causes ... vomiting • Late (shock ... a scrotum #21HydroxylaseDeficiency ... endocrinology #peds ... #pediatrics
Childhood Immunization Schedule: Why we immunize • Diphtheria Toxin -> URT inflammation causes pseudomembrane with hardened
& hemorrhagic rash ... ; symptoms of shock ... Vesicular & pruritic rash ... #Immunization #peds ... #pediatrics #pathophysiology
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