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Behcet Syndrome

More information in Books or onNLM PubMed
Definition: Rare chronic inflammatory disease involving the small blood vessels. It is of unknown etiology and characterized by mucocutaneous ulceration in the mouth and genital region and uveitis with hypopyon. The neuro-ocular form may cause blindness and death. SYNOVITIS; THROMBOPHLEBITIS; gastrointestinal ulcerations; RETINAL VASCULITIS; and OPTIC ATROPHY may occur as well.  in translations spell Beh+šet's, not Behcet's    Other names Triple-Symptom Complex; Behcet's Syndrome; Behcet Disease; Triple Symptom Complex; Behcets Syndrome
 
SubstanceCAS Registry & nameCategoriesSource
BES-1 protein, Streptococcus sanguis  0   *Antigens, Bacterial Behcet Syndrome. Zentralbl Bakteriol 1998 May;287(4):449-60

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Sources: NLM Medical Subject Headings, NIH UMLS, Drugs@FDA, FDA AERS original data copyright United States Government. No endorsement implied. Last modified 6/6/2012

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