The Calgary Guide to Understanding Disease @TheCalgaryGuide
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pathophysiology pediatrics 21hydroxylasedeficiency childhood endocrinology genetics
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 ... endocrinology #peds
Childhood Immunization Schedule: Why we immunize • Diphtheria Toxin -> URT inflammation causes pseudomembrane with hardened
Childhood Immunization ... hemorrhagic rash; symptoms ... encephalitis and cellulitis ... non-specific viral symptoms ... #peds #pediatrics
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