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21hydroxylasedeficiency diagnosis genetics management nutrition pediatrics peds scurvy vitaminc
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 ... #21HydroxylaseDeficiency #21OHD ... #pathophysiology ... #genetics #endocrinology
Scurvy (Vitamin C Deficiency) - Diagnosis and Management Vitamin C is required for hydroxylation of proline residues
Psychiatric symptoms ... beta-spectrin, which is crucial ... , or any other cause ... #VitaminC #AscorbicAcid ... #Pathophysiology
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