provides a comprehensive look
at the who, what, when and how of Behcet's syndrome
< b>Behcet's syndrome: A chronic inflammatory disorder involving the small
blood vessels which is characterized by a classic triad of features: ulcers in the
mouth, ulcers of the genitalia, and inflammation of the eye (uveitis). The mouth
and genital ulcers recur in crops and are painful. The mouth ulcers appear on the
inner lining of the mouth, the gums, and tongue. The genital ulcers occur on the
scrotum and penis of males and vulva of women and can leave scars. Arthritis is
commonplace with Behcet's syndrome, as is involvement of the gastrointestinal system
and central nervous system. The cause of Behcet's syndrome is not known. It is more
frequent and severe in patients from the Eastern Mediterranean and Asia than those
of European descent. Treatment for Behcet's disease is symptomatic and supportive.
Medication may be prescribed to reduce inflammation and suppress the immune system.
Named for the Turkish dermatologist Halushi Behcet (1889-1948). Also known as
Silk Road disease.
Common Misspellings: behcet's syndrone, bechets syndrome, bechets syndrone
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