Behcet's disease

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Behçet's disease

Behçet syndrome An idiopathic multisystem condition most common in the Middle East; ♂:♀ ratio 2:1, aged 15–40 Clinical Pustules, aphthous stomatitis–90%, genital ulcers; vasculitis; erythema nodosa–80%, meningoencephalitis, synovitis, uveitis Lab ↑ ESR, ↑ Igs, anemia Management Symptomatic, corticosteroids
References in periodicals archive ?
(15.) Batioglu F, Atmaca LS, Karabulut HG et al: Factor V leiden and prothtombin gene G20210A mutations in ocular Behcet disease. Acta Ophtalmol Scand 2003:81;283-5.
Evereklioglu, "The migration pattern, patient selection with diagnostic methodological flaw and confusing naming dilemma in Behcet disease," European Journal of Echocardiography, vol.
Ishibashi, "Therapeutic neutrophil apheresis in patients with ocular Behcet disease," Archives of Ophthalmology, vol.
Aortic and arterial aneurysms in behcet disease: management with stent-grafts--initial experience.
Serum prolactin levels and Behcet disease. Eur J Ophthalmol 2007;17:404-7.
Major vessel involvement in Behcet disease. Curr Opin Rheumatol 2005;17:1-8.
Infliksimab for the treatment of posterior uveitis with retinal neovascularization in Behcet disease. Eur J Ophthalmol 2004; 14: 445-8.
Patients with Behcet disease have been subclassified into various clusters on the basis of clinical expressions (1).
Neurological involvement in North Italian patients with Behcet disease. Rheumatol Int 2006;26: 1113-9.