Behçet syndrome is a rare, chronic inflammatory disease of unknown aetiopathogenesis,
most commonly presenting with mucocutaneous and ocular manifestations. Vascular …

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 …

Behçet's disease (BD) is a chronic, relapsing inflammatory, multisystem disease of unknown
etiology. The disease has a wide clinical spectrum of mucocutaneous lesions and ocular …

Abstract Purpose of Review To assess current management of Behcet's disease (BD).
Controversies on therapeutic approaches to different manifestations, whether conventional …

Behçet syndrome (BS) is a unique type of vasculitis that affects veins and arteries of all
sizes, leading to recurrent vascular events, mostly venous thrombosis. The prevalence of …

Behcet's Disease was first described by a Turkish dermatologist, Hulusi Behcet, in 1937 as a
triple symptom complex; aphthous stomatitis, genital ulcers, and uveitis. Today, in light of …

Behçet's syndrome (BS) is a complex disease that shows important heterogeneity in clinical
findings and physiopathology. Its treatment can be problematic as BS manifestations in …

Objectives Behçet's syndrome (BS) is a rare systemic vasculitis often complicated by
thrombotic events. Given the lack of validated biomarkers, BS diagnosis relies on clinical …

Behçet disease (BD) is a complex, multi-systemic inflammatory condition mainly hallmarked
by oral and genital ulcers which can also affect the vessels, gastrointestinal tract, central …

Objectives Both innate and adaptive immune responses are reportedly increased in
Behçet's disease (BD), a chronic, relapsing systemic vasculitis lying at the intersection …