Behçet's Disease (BD) is an inflammatory disease of unknown etiology with multisystemic
involvement, being the main clinical manifestations represented by recurrent oral and …

Behçet's disease is a rare and poorly understood vasculitis affecting blood vessels of all
types and sizes. Uveitis and oral and genital ulcers represent the typical clinical triad …

Behçet's disease (BD) is a chronic, vasculitic disorder affecting all sizes of vessels. The
disease rarely onsets at childhood and an early diagnosis is often challenging. Oral …

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 …

BD is a systemic inflammatory disease with a variable vasculitis. Paediatric onset is very rare
and carries a strong genetic component. Oral ulcers and fever of unknown origin are …

Background Behçet's disease is a rare multi-systemic inflammatory disease with unknown
etiology which involves principally oral and genital mucosa, skin and eyes. Average age at …

Behçet's disease is an inflammatory vasculitic disease of unknown etiology characterized by
recurrent oral and genital ulcers, ocular findings, and multiple organ involvement …

Behçet's disease (BD) is a variable vessel vasculitis characterized by recurrent oral and
genital aphthosis accompanied by skin, ocular, gastrointestinal, neurologic, and articular …

There are currently limited data regarding paediatric Behçet's disease (BD), particularly in
the UK. We describe the clinical spectrum, treatment and outcome of BD, and explore the …

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 …