Gender Differences in Behçet’s Disease Associated Uveitis

Behçet’s disease is a systemic vasculitis of unknown etiology, characterized by oral and genital ulceration, skin lesions, and uveitis as well as vascular, central nervous system, and gastrointestinal system involvement. It is prevalent in the Middle East, Mediterranean, and Eastern Asia. The aim of...

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Main Authors: Didar Ucar-Comlekoglu, Austin Fox, H. Nida Sen
Format: Article
Language:English
Published: Wiley 2014-01-01
Series:Journal of Ophthalmology
Online Access:http://dx.doi.org/10.1155/2014/820710
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author Didar Ucar-Comlekoglu
Austin Fox
H. Nida Sen
author_facet Didar Ucar-Comlekoglu
Austin Fox
H. Nida Sen
author_sort Didar Ucar-Comlekoglu
collection DOAJ
description Behçet’s disease is a systemic vasculitis of unknown etiology, characterized by oral and genital ulceration, skin lesions, and uveitis as well as vascular, central nervous system, and gastrointestinal system involvement. It is prevalent in the Middle East, Mediterranean, and Eastern Asia. The aim of this review is to evaluate the gender differences in clinical manifestations of Behçet’s disease, treatment responses, mortality, and morbidity. Behçet’s disease has been reported to be more prevalent in males from certain geographic regions and particular ethnic groups; however, recent reports indicate more even gender distribution across the world. There are gender differences in clinical manifestations and severity of the disease. Ocular manifestations, vascular involvement, and neurologic symptoms are more frequently reported in male patients whereas oral and genital ulcers, skin lesions, and arthritis occur more frequently in female patients. The disease can have a more severe course in males, and overall mortality rate is significantly higher among young male patients.
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institution Kabale University
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series Journal of Ophthalmology
spelling doaj-art-0b7abe3d626049b68eaffdf37659c92f2025-02-03T05:59:45ZengWileyJournal of Ophthalmology2090-004X2090-00582014-01-01201410.1155/2014/820710820710Gender Differences in Behçet’s Disease Associated UveitisDidar Ucar-Comlekoglu0Austin Fox1H. Nida Sen2National Eye Institute, National Institutes of Health, Bethesda, MD 20892, USANational Eye Institute, National Institutes of Health, Bethesda, MD 20892, USANational Eye Institute, National Institutes of Health, Bethesda, MD 20892, USABehçet’s disease is a systemic vasculitis of unknown etiology, characterized by oral and genital ulceration, skin lesions, and uveitis as well as vascular, central nervous system, and gastrointestinal system involvement. It is prevalent in the Middle East, Mediterranean, and Eastern Asia. The aim of this review is to evaluate the gender differences in clinical manifestations of Behçet’s disease, treatment responses, mortality, and morbidity. Behçet’s disease has been reported to be more prevalent in males from certain geographic regions and particular ethnic groups; however, recent reports indicate more even gender distribution across the world. There are gender differences in clinical manifestations and severity of the disease. Ocular manifestations, vascular involvement, and neurologic symptoms are more frequently reported in male patients whereas oral and genital ulcers, skin lesions, and arthritis occur more frequently in female patients. The disease can have a more severe course in males, and overall mortality rate is significantly higher among young male patients.http://dx.doi.org/10.1155/2014/820710
spellingShingle Didar Ucar-Comlekoglu
Austin Fox
H. Nida Sen
Gender Differences in Behçet’s Disease Associated Uveitis
Journal of Ophthalmology
title Gender Differences in Behçet’s Disease Associated Uveitis
title_full Gender Differences in Behçet’s Disease Associated Uveitis
title_fullStr Gender Differences in Behçet’s Disease Associated Uveitis
title_full_unstemmed Gender Differences in Behçet’s Disease Associated Uveitis
title_short Gender Differences in Behçet’s Disease Associated Uveitis
title_sort gender differences in behcet s disease associated uveitis
url http://dx.doi.org/10.1155/2014/820710
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