Behçet disease (Q44396): Difference between revisions

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Doença de Behçet é uma doença de etiopatogenia não completamente compreendida caracterizada por úlceras aftosas orais e/ou genitais recorrentes acompanhadas de lesões inflamatórias cutâneas, oculares, articulares, gastrointestinais e/ou do sistema nervoso central. Podem ocorrer vasculites de pequenos vasos, vasculopatia trombótica, arterites e aneurismas arteriais. Tem uma alta prevalência do Mediterrâneo Oriental através de toda a Ásia Central até a China e Japão.
description / endescription / en
 
Behçet disease is a disease of incompletely understood aetiopathogenesis characterised by recurrent oral and/or genital aphthous ulcers accompanied by cutaneous, ocular, articular, gastrointestinal, and/or central nervous system inflammatory lesions. Small vessel vasculitis, thrombotic vasculopathy, arteritis and arterial aneurysms may occur. It has a high prevalence from the Eastern Mediterranean across Central Asia to China and Japan.

Revision as of 11:50, 13 August 2026

Behçet disease is a disease of incompletely understood aetiopathogenesis characterised by recurrent oral and/or genital aphthous ulcers accompanied by cutaneous, ocular, articular, gastrointestinal, and/or central nervous system inflammatory lesions. Small vessel vasculitis, thrombotic vasculopathy, arteritis and arterial aneurysms may occur. It has a high prevalence from the Eastern Mediterranean across Central Asia to China and Japan.
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4A62
    English
    Behçet disease
    Behçet disease is a disease of incompletely understood aetiopathogenesis characterised by recurrent oral and/or genital aphthous ulcers accompanied by cutaneous, ocular, articular, gastrointestinal, and/or central nervous system inflammatory lesions. Small vessel vasculitis, thrombotic vasculopathy, arteritis and arterial aneurysms may occur. It has a high prevalence from the Eastern Mediterranean across Central Asia to China and Japan.

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