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21hydroxylasedeficiency diagnosis extraarticular genetics pediatrics peds ra rheumatoidarthritis symptoms
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
Signs/Symptoms/Complications ... may look like a penis ... #21HydroxylaseDeficiency #21OHD ... #pathophysiology ... #genetics #endocrinology
Rheumatoid arthritis (RA): Extra-articular manifestations Skin: • Inflammation of skin (esp. over areas of stress) forms
blood vessels (vasculitis ... RA inflammation tends ... RheumatoidArthritis #RA #pathophysiology ... #signs #symptoms
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