Satellite skin ucsdh pathophysiology endocrinology pediatrics childhood - GrepMed

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21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings
Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase

cold & mottled skin ... #21HydroxylaseDeficiency #21OHD #pathophysiology ... #genetics #endocrinology ... #peds #pediatrics

Childhood Immunization Schedule: Why we immunize
• Diphtheria Toxin -> URT inflammation causes pseudomembrane with hardened

Childhood Immunization ... that persists as skin ... discharge #Childhood ... Immunization #peds #pediatrics ... #pathophysiology

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