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Behçet's disease: Difference between revisions
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{{disease|Behçet|M35.2}} | |||
Behçet's disease or Behçet disease, sometimes called Behçet's syndrome, Morbus Behçet, Behçet-Adamantiades syndrome, or Silk Road disease, is a rare immune-mediated small-vessel systemic vasculitis that often presents with mucous membrane ulceration and ocular problems. Behçet's disease (BD) was named in 1937 after the Turkish dermatologist [[Hulusi Behçet]], who first described the triple-symptom complex of recurrent oral aphthous ulcers, genital ulcers, and uveitis. | Behçet's disease or Behçet disease, sometimes called Behçet's syndrome, Morbus Behçet, Behçet-Adamantiades syndrome, or Silk Road disease, is a rare immune-mediated small-vessel systemic vasculitis that often presents with mucous membrane ulceration and ocular problems. Behçet's disease (BD) was named in 1937 after the Turkish dermatologist [[Hulusi Behçet]], who first described the triple-symptom complex of recurrent oral aphthous ulcers, genital ulcers, and uveitis. | ||
[[nl:Ziekte van Behçet]] | [[nl:Ziekte van Behçet]] | ||
Revision as of 17:54, 28 July 2015
Disease classification WHO
Behçet M35.2
Behçet's disease or Behçet disease, sometimes called Behçet's syndrome, Morbus Behçet, Behçet-Adamantiades syndrome, or Silk Road disease, is a rare immune-mediated small-vessel systemic vasculitis that often presents with mucous membrane ulceration and ocular problems. Behçet's disease (BD) was named in 1937 after the Turkish dermatologist Hulusi Behçet, who first described the triple-symptom complex of recurrent oral aphthous ulcers, genital ulcers, and uveitis.