Behçet's disease is characterized with recurrent attacks of inflammation that are driven by
systemic vasculitis without any clearly demonstrated triggering mechanism. It is more …

Behçet disease is a systemic vasculitis with an unknown etiology that affects vessels of all
sizes and types. Mucocutaneous lesions that include oral aphthous ulcers, genital ulcers …

Behçet's disease (BD) is a chronic, relapsing, systemic inflammatory vasculitis of unknown
aetiology with a myriad of immunological and pathological consequences. Patients with BD …

Behçet's disease is a systemic vasculitis of unknown aetiology characteristically affecting
venules. Onset is typically in young adults with recurrent oral and genital ulceration, uveitis …

Behçet's disease (BD) is an idiopathic, chronic, relapsing, multi-systemic vasculitis
characterized by recurrent oral and genital aphthous ulcers, ocular disease and skin lesions …

Behçet's disease (BD) is a systemic vasculitis of unknown etiology involving the small and
large vessels of both the venous and arterial systems. This disease, first recognized to be a …

Behçet's disease is an autoinflammatory vasculitis of unknown origin characterized by
recurrent oral and genital ulcers, uveitis, arthritis and skin lesions. Additionally, involvement …

Behcet disease (BD) was first described by a Turkish dermatologist as a triplesymptom
complex that consists of oral aphthous ulcers, genital ulcers, and uveitis. It is now …

Behçet's disease is an immune-mediated vasculitis affecting both small and large vessels.
Small-vessel vasculitis is the pathological basis of the multiorgan involvement that results in …

Background: Behçet's disease (BD) is an idiopathic, chronic, relapsing, multi-systemic
vasculitis characterized by recurrent oral and genital aphthous ulcers, ocular disease and …