| 영문 | Behcet disease | 한글 | 베체트병 |
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| 설명 | 심한 포도막염, 망막혈관염, 시각신경위축, 구강-성기의 아프타성 궤양, 광범위한 혈관염의 징후와 증상을 나타낸다. 원인불명의 희귀한 병으로 젊은 남자에게 잘 발생한다. |
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| BD | Behcet's Disease |
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| BS | Behcet's Syndrome |
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| Behcet's disease | <syndrome> A multisystem, chronic recurrent disease characterised by ulceration in the mouth and genitalia, iritis, uveitis, arthritis and thrombophlebitis. Often treated with immunosuppressive therapy (corticosteroids, chlorambucil). (27 Sep 1997) |
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| Behcet's syndrome | <syndrome> A multisystem, chronic recurrent disease characterised by ulceration in the mouth and genitalia, iritis, uveitis, arthritis and thrombophlebitis. Often treated with immunosuppressive therapy (corticosteroids, chlorambucil). (27 Sep 1997) |
| Behcet | Hulusi, Turkish dermatologist, 1889-1948. See: Behcet's disease, Behcet's syndrome. (05 Mar 2000) |
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| syndrome, behcet's | Behcet's syndrome is classically characterised as a triad of symptoms that include recurring crops of mouth ulcers (called apthous ulcers), genital ulcers, and inflammation of a specialised area around the pupil of the eye, the uvea. (the inflammation is called uveitis.) the cause of behcet's syndrome is not known. The disease is more frequent and severe in patients from the eastern mediterranean and asia than those of european descent. (12 Dec 1998) |
| Behcet's syndrome |
is characterised by painful oral and genital ulcers, inflammatory eye disease, and skin lesions. It is a rare disorder in Europe and America but more common in Japan and some Middle Eastern countries.
출처: www.arc.org.uk/about_arth/glossary.htm
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| Behcet's syndrome |
Orogenital ulceration, arthritis and other clinical (frequently vascular) features. More common in the Eastern Mediterranean area and Japan than elsewhere.
출처: www.ilar.org/Glossary/Glossary_b.htm
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제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
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제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
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