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 is a rare vasculitis diagnosed by the presence of recurrent oral ulcers and
two of the following: genital ulcers, typical eye lesions, typical skin lesions, and positive …

Background: Behcet's disease (BD) is a complex inflammatory vascular disorder that follows
a relapsing-remitting course with diverse clinical manifestations. The prevalence of the …

An update on the diagnosis, treatment, and prognosis of inte... : Current Opinion in
Rheumatology An update on the diagnosis, treatment, and prognosis of intestinal Behçet's …

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 disease is a chronic inflammatory systemic disorder, characterized by a relapsing
and remitting course. It manifests with oral and genital ulcerations, skin lesions, uveitis, and …

Behçet syndrome (also known as Behçet disease) is a rare condition that is associated with
considerable morbidity. Cases of Behçet syndrome have been reported worldwide, but the …

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 (BD) is a systemic vasculitis disorder of unknown etiology, characterized
by relapsing episodes of oral aphthous ulcers, genital ulcers, skin lesions and ocular …

Definition of the disease Behçet disease (BD) is a chronic, relapsing, multisystemic disorder
characterized by mucocutaneous, ocular, vascular and central nervous system …