Behcets disease is a rare immune-mediated small-vessel systemic vasculitis that often presents with mucous membrane ulceration and ocular problems. The disease was named in 1937 after the Turkish dermatologist Hulusi Behcet, who first described the triple-symptom complex of recurrent oral aphthous ulcers, genital ulcers, and uveitis – a disease of the eye. As a systemic disease, it can also involve visceral organs such as the gastrointestinal tract, pulmonary, musculoskeletal, cardiovascular and neurological systems. This syndrome can be fatal due to ruptured vascular aneurysms or severe neurological complications
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al-mujaini a, wali uk. frosted branch angiitis, neuroretinitis as initial ocular manifestation in behçet disease. indian j ophthalmol [serial online] 2011 [cited 2016 dec 18];59:240-1. available from: http://www.ijo.in/text.asp?2011/59/3/240/81048