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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Published in | Current rheumatology reviews Vol. 17; no. 3; p. 360 |
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Main Authors | , , , |
Format | Journal Article |
Language | English |
Published |
United Arab Emirates
01.01.2021
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Subjects | |
Online Access | Get more information |
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