Helvaci, Mehmet RamiÖzcura, FatihHacio?lu, AlperÇivi, Kismet2024-09-192024-09-1920081300-0292https://hdl.handle.net/20.500.12483/14526Behçet's disease is a systemic vasculitis, dominated clinically by recurrent oral and genital ulcerations, uveitis, and erythema nodosum-like cutaneous lesions. However, widespread organ involvement is now well recognized, and geo-graphic and ethnic variations of the clinical manifestations are common. The majority of the affected individuals do not have a life-threatening disease, but mortality can be increased with vascular and/or thrombotic complications. Although ocular involvement occurs approximately in 70% of patients, clinically presented retinal vascular events are rare in the disease. We report a Behçet's case, initially diagnosed with a right-sided central retinal vein occlusion in the absence of uveitis as a rare presentation and a short review of the literature. Copyright © 2008 by Türkiye Klinikleri.eninfo:eu-repo/semantics/closedAccessBehçet syndromeRetinal vein occlusionArticle2834034072-s2.0-46749145725Q4