Introduction Behçet's disease (BD) is an auto-inflammatory disease, primarily characterized
by recurrent painful mucocutaneous ulcerations. Methods A literature search was performed …

The presence of symptom clusters, regional differences in disease expression and
similarities with, for example, Crohn's disease suggest multiple pathological pathways are …

Behçet's disease (BD) is a rare systemic vasculitis characterized by oral aphthous ulcers,
genital ulcers, ocular lesions and other systemic manifestations. BD occurs most frequently …

Behçet disease (BD) is a chronic inflammatory multisystem disease characterized by oral
and genital ulcers, uveitis, and skin lesions. Disease etiopathogenesis is still unclear. We …

Objective. To review the progress in the field of MHC-related genetic susceptibility to
Behçet's disease (BD). Method. Systematic review of the English literature between 1 …

Behçet's disease is a systemic vasculitis characterized by recurrent oral and genital ulcers,
and ocular inflammation, and which may involve the joints, skin, central nervous system and …

Behcet's disease (BD) is a systemic inflammatory disorder with a diverse spectrum of clinical
manifestations including mucocutaneous, ocular, vascular, gastrointestinal, musculoskeletal …

Behcet's syndrome (BS) is a vasculitis, seen more commonly around the Mediterranean and
the Far East, and manifests with oral and genital ulcerations, skin lesions, uveitis, and …

Behçet disease (BD) is a multisystem inflammatory disorder of unknown etiology. BD has a
multifactorial pathogenesis, and genetics plays a critical role in the development of the …

Behçet syndrome is a systemic vasculitis with an unknown aetiology affecting the small and
large vessels of the venous and arterial systems. The presence of symptom clusters …