Afib diagnosis symptoms peds causes clinical video pediatrics management infant ascorbicacid 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

Pathogenesis and Clinical ... enzyme 21-OHase causes ... Signs/Symptoms/Complications ... endocrinology #peds ... #pediatrics

Scurvy (Vitamin C Deficiency) - Diagnosis and Management

Vitamin C is required for hydroxylation of proline residues

and Management ... eating habits • Infants ... poor nutrition Clinical ... , or any other cause ... Pathophysiology #VitaminC #AscorbicAcid

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