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Behçet disease (BD) is a type of vasculitis with relapsing episodes and multisystemic clinical features. Symptoms include oral ulcers as well as a range of manifestations that can involve the articular, neurologic, ocular, vascular, gastrointestinal, urogenital, pulmonary, and cardiac systems [1,2]. Although rare, BD affects people from around the world, and it is relatively more common among patients from the Silk Road demographic (including regions in the Middle East and Asia) [1,3].
JMIR Form Res 2023;7:e49380
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Stevens-Johnson Syndrome in Adult Patient Secondary to COVID-19 Infection: Case Report
vasculitis
JMIR Dermatol 2023;6:e45062
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The aims of this study were to describe the self-reported clinical features of patients with granulomatosis with polyangiitis and microscopic polyangiitis who participated in the Vasculitis Patient-Powered Research Network and to establish to what extent this internet-based cohort is representative of the general population of patients with these forms of antineutrophil cytoplasmic antibody–associated vasculitis.
J Med Internet Res 2020;22(7):e17231
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