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diagnosis symptoms 21hydroxylasedeficiency criteria dermatomyositis disease dm endocrinology genetics kawasaki pediatrics peds pm polymyositis
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
Pathogenesis and Clinical ... Signs/Symptoms/Complications ... cold & mottled skin ... #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,
Pathogenesis and clinical ... processes occur in the skin ... PM #Diagnosis #Pathophysiology ... #Signs #Symptoms ... #Vasculitis
Kawasaki Disease: Clinical Findings Diagnostic Criteria - Fever and 4/5 of the following: • Conjunctivitis • Polymorphous
Kawasaki Disease: Clinical ... hands & feet Signs ... - Generalized Skin ... Criteria #Diagnosis #Pathophysiology ... #Vasculitis
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