Refractory Behçet's Disease with Multi-organ Involvement - Learning from Failure

Behçet's disease (BD) is a rare systemic vasculitis of unknown etiology with relapsing and remitting course, characterized by triple-symptom complex of recurrent attacks of oral aphthous ulcers, genital ulcers and ocular lesions and other clinical features that include dermatological, cardiovas...

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Bibliographic Details
Published inCurrent rheumatology reviews Vol. 17; no. 3; p. 360
Main Authors Santos, Christiana Sieiro, Morales, Clara Moriano, Álvarez, Elvira Díez, Sandoval, Trinidad Pérez
Format Journal Article
LanguageEnglish
Published United Arab Emirates 01.01.2021
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