A Behcet's case presenting with central retinal vein occlusion: Case report

dc.contributor.authorHelvaci, Mehmet Rami
dc.contributor.authorOezcura, Fatih
dc.contributor.authorHacioglu, Alper
dc.contributor.authorCivi, Kismet
dc.date.accessioned2024-09-18T20:04:22Z
dc.date.available2024-09-18T20:04:22Z
dc.date.issued2008
dc.departmentHatay Mustafa Kemal Üniversitesien_US
dc.description.abstractBehcet'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.en_US
dc.identifier.endpage407en_US
dc.identifier.issn1300-0292
dc.identifier.issn2146-9040
dc.identifier.issue3en_US
dc.identifier.startpage403en_US
dc.identifier.urihttps://hdl.handle.net/20.500.12483/8116
dc.identifier.volume28en_US
dc.identifier.wosWOS:000257362400022en_US
dc.identifier.wosqualityN/Aen_US
dc.indekslendigikaynakWeb of Scienceen_US
dc.language.isoenen_US
dc.publisherOrtadogu Ad Pres & Publ Coen_US
dc.relation.ispartofTurkiye Klinikleri Tip Bilimleri Dergisien_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectBehcet syndromeen_US
dc.subjectretinal vein occlusionen_US
dc.titleA Behcet's case presenting with central retinal vein occlusion: Case reporten_US
dc.typeArticleen_US

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