Trigger pathophysiology differential peds symptoms pediatrics neonatal jaundice congenital 21ohd

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

also known as "congenital ... Signs/Symptoms/Complications ... #pathophysiology ... endocrinology #peds ... #pediatrics

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

hemorrhagic rash; symptoms ... organ ischemia -> Congenital ... anorexia, nausea, jaundice ... #Immunization #peds ... #pediatrics #pathophysiology

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