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

Neuro-Behcet's disease (NBD) is defined as a combination of neurologic symptoms and/or
signs in a patient with Behcet's disease (BD). Relevant syndromes include brainstem …

Behçet's disease is a multisystem disorder with unknown etiology and a unique geographic
distribution. The disease is characterized by recurrent skin–mucosa lesions and sight …

Objectives The association between mutations in TNFAIP3, encoding the NF-kB regulatory
protein A20, and a new autoinflammatory disease has recently been recognised. This study …

Behçet's disease (BD) is a systemic variable vessel vasculitis that involves the skin, mucosa,
joints, eyes, arteries, veins, nervous system and gastrointestinal system, presenting with …

Behçet's Disease (BD) is a systemic vasculitis firstly described as a disorder causing
aphthous lesion in oral and genital mucosae and uveitis. The disease has an extremely …

Behçet syndrome (BS) is an idiopathic chronic relapsing multisystem vascular-inflammatory
disease of unknown origin. As the disease affects many organs and systems and shows a …

Behcet's syndrome (BS) is a chronic, recurrent relapsing multisystem vascular-inflammatory
syndrome of unknown etiology that predominantly affects veins. Although BS was initially …

Autoinflammatory diseases (AID) are diseases of the innate immune system, characterized
by recurrent episodes of localized or systemic inflammation. Vasculitis may accompany AID …

Behçet's syndrome (BS) is a multisystem vasculitis that presents with a variety of
mucocutaneous manifestations such as oral and genital ulcers, papulopustular lesions and …