The Calgary Guide to Understanding Disease @TheCalgaryGuide
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21hydroxylasedeficiency diagnosis hsp iga pediatrics peds signs symptoms
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
#21HydroxylaseDeficiency #21OHD ... #pathophysiology ... #genetics #endocrinology ... #peds #pediatrics
IgA Vasculitis – Henoch Scholein Purpura: Pathogenesis and Clinical Findings - Infectious Agents - 50% have
IgA Vasculitis – ... predisposition - Various genetic ... #HSP #IgA #Vasculitis ... #HenochScholeinPurpura ... #Pathophysiology
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