- Behçet's syndrome facts
- What is Behçet's syndrome?
- What are symptoms of Behçet's syndrome?
- How is Behçet's syndrome diagnosed?
- What is the treatment of Behçet's syndrome?
- Patient Comments: Behcet's Syndrome - Symptoms
- Patient Comments: Behcet's Syndrome - Effective Treatments
- Patient Comments: Behcet's Syndrome - Experience
Behçet's syndrome facts
- Behçet's syndrome is associated with inflammation of various areas of the body.
- Symptoms of Behçet's syndrome depend on the body areas affected.
- Recurrent mouth ulcers are characteristic of Behçet's syndrome.
- Treatment of Behçet's syndrome depends on the severity and the location of its manifestations.
What is Behçet's syndrome?
Behçet's syndrome is classically characterized as a triad of symptoms that include recurring crops of mouth ulcers (aphthous ulcers, canker sores), genital ulcers, and inflammation of a specialized area around the pupil of the eye termed the uvea. The inflammation of the area of the eye that is around the pupil is called uveitis. Behçet's syndrome is also sometimes referred to as Behçet's disease.
The cause of Behçet's syndrome is not known. The disease is relatively rare but is more frequent and severe in patients from the Eastern Mediterranean and Asia than those of European descent. Both inherited (genetic) and environmental factors, such as microbe infections, are suspected to be factors that contribute to the development of Behçet's syndrome. Behçet's syndrome is not proven to be contagious.
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