Behçet's disease natural history, complications and prognosis: Difference between revisions
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__NOTOC__ | __NOTOC__ | ||
{{Behçet's disease}} | {{Behçet's disease}} | ||
{{CMG}} | {{CMG}}; {{AE}} {{HQ}} | ||
==Overview== | ==Overview== | ||
==Natural History, Complications, and Prognosis== | ==Natural History, Complications, and Prognosis== | ||
Revision as of 23:24, 1 May 2018
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Hamid Qazi, MD, BSc [2]
Overview
Natural History, Complications, and Prognosis
Natural History
- The symptoms of Behcet disease usually develop in the second to third decade of life, and start with symptoms such as uveitis, mouth sores, and skin lesions.
Complications
- Common complications of Behcet disease include:
- Neuro Behcet
- Vision loss
- Aneurysm
Prognosis
- Depending on the extent of the disease at the time of diagnosis, the prognosis may vary. However, the prognosis is generally regarded as good.
- The worst prognoses are associated with retinal vasculitis, leading to blindness; vascular aneurysm formation, with possible rupture; and neuro–Behçet syndrome, which may lead to dementia despite appropriate aggressive treatment.