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diagnosis symptoms 21hydroxylasedeficiency dermatomyositis endocrinology extraarticular genetics pediatrics peds pm polymyositis ra rheumatoidarthritis
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
Signs/Symptoms/Complications ... scrotum & enlarged penis ... may look like a penis ... #21HydroxylaseDeficiency #21OHD ... #pathophysiology
Dermatomyositis (DM) and Polymyositis (PM): Pathogenesis and clinical findings Elevated Antinuclear Antibodies: Anti-Jo-1, Anti-OJ, Anti-Mi2, Anti-SRP, Anti-EJ,
Dermatomyositis (DM ... Dermatomyositis #DM ... PM #Diagnosis #Pathophysiology ... #Signs #Symptoms ... #Vasculitis
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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