Helvaci, Mehmet RamiOezcura, FatihHacioglu, AlperCivi, Kismet2024-09-182024-09-1820081300-02922146-9040https://hdl.handle.net/20.500.12483/8116Behcet'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 Behcet'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.eninfo:eu-repo/semantics/closedAccessBehcet syndromeretinal vein occlusionArticle283403407WOS:000257362400022N/A