PCL diagnosis pathophysiology peds symptoms causes pediatrics msk infant newborn 21ohd ascorbicacid

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

enzyme 21-OHase causes ... Signs/Symptoms/Complications ... #pathophysiology ... endocrinology #peds ... #pediatrics

Scurvy (Vitamin C Deficiency) - Diagnosis and Management

Vitamin C is required for hydroxylation of proline residues

Deficiency) - Diagnosis ... eating habits • Infants ... nonimmune hemolysis MSK ... , or any other cause ... #VitaminC #AscorbicAcid

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