Behcet Syndrome

Overview

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.

This information is general and should not be treated as medical advice. Always speak directly with a qualified healthcare professional before making decisions about treatment, diagnosis, procedures, medicines or care.

Quick facts about Behcet Syndrome

Topic type

Condition

Category

Dentistry

MeSH classification

C07.465.075|C11.941.879.780.880.200|C14.907.940.100|C16.320.382.250|C17.800.827.368.250|C17.800.862.150

Preparing for an appointment about Behcet Syndrome

If you are speaking with a healthcare professional about Behcet Syndrome, it can help to prepare a few details in advance.

• Write down your symptoms and when they started.
• Bring details of any medicines, supplements or previous treatments.
• Ask what tests or assessments may be needed.
• Ask what treatment or management options may be suitable.
• Ask when you should seek urgent medical help or follow-up care.

Finding care related to Behcet Syndrome

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