"Behcet Syndrome" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
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.
| Descriptor ID |
D001528
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| MeSH Number(s) |
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
|
| Concept/Terms |
Behcet Syndrome- Behcet Syndrome
- Triple-Symptom Complex
- Behcet Disease
- Triple Symptom Complex
- Complex, Triple Symptom
- Complices, Triple Symptom
- Symptom Complex, Triple
- Symptom Complices, Triple
- Triple Symptom Complices
- Adamantiades-Behcet Disease
- Adamantiades Behcet Disease
- Adamantiades-Behcet Diseases
- Disease, Adamantiades-Behcet
- Diseases, Adamantiades-Behcet
- Behcet Triple Symptom Complex
- Old Silk Route Disease
- Behcet's Syndrome
- Behcets Syndrome
- Behçet Disease
- Behçet Diseases
- Disease, Behçet
- Diseases, Behçet
|
Below are MeSH descriptors whose meaning is more general than "Behcet Syndrome".
Below are MeSH descriptors whose meaning is more specific than "Behcet Syndrome".
This graph shows the total number of publications written about "Behcet Syndrome" by people in this website by year, and whether "Behcet Syndrome" was a major or minor topic of these publications.
To see the data from this visualization as text,
click here.
| Year | Major Topic | Minor Topic | Total |
|---|
| 2001 | 1 | 1 | 2 |
| 2005 | 1 | 0 | 1 |
| 2012 | 1 | 0 | 1 |
| 2013 | 0 | 1 | 1 |
| 2017 | 2 | 0 | 2 |
| 2020 | 1 | 0 | 1 |
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click here.
Below are the most recent publications written about "Behcet Syndrome" by people in Profiles.
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Manthiram K, Preite S, Dedeoglu F, Demir S, Ozen S, Edwards KM, Lapidus S, Katz AE, Feder HM, Lawton M, Licameli GR, Wright PF, Le J, Barron KS, Ombrello AK, Barham B, Romeo T, Jones A, Srinivasalu H, Mudd PA, DeBiasi RL, G?l A, Marshall GS, Jones OY, Chandrasekharappa SC, Stepanovskiy Y, Ferguson PJ, Schwartzberg PL, Remmers EF, Kastner DL. Common genetic susceptibility loci link PFAPA syndrome, Beh?et's disease, and recurrent aphthous stomatitis. Proc Natl Acad Sci U S A. 2020 06 23; 117(25):14405-14411.
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Starr MR, Smith WM. A Teenage Girl With Aseptic Meningitis and Unilateral Blurry Vision. JAMA Ophthalmol. 2017 10 01; 135(10):1111-1112.
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Gurunathan A, Teachey DT, Chikwava KR, Witmer C, Desai AV. Behcet Disease Initially Presenting as Deep Venous Thrombosis: A Case Report. J Pediatr Hematol Oncol. 2017 07; 39(5):410-412.
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Hasan N, Bagga S, Monteagudo J, Hirose H, Cavarocchi NC, Hehn BT, Kavuru MS. Extracorporeal membrane oxygenation to support whole-lung lavage in pulmonary alveolar proteinosis: salvage of the drowned lungs. J Bronchology Interv Pulmonol. 2013 Jan; 20(1):41-4.
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Jafri L, Nasir N, Almas A. Multifocal venous thrombosis in Behcet's disease. J Coll Physicians Surg Pak. 2012 Nov; 22(11):730-2.
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Jarrahnejad P, Gadepalli S, Zurkovsky E, Tulsyan N, Rolandelli R. Behcet's disease: a rare cause of lower gastrointestinal bleeding. Int J Colorectal Dis. 2006 Dec; 21(8):856-8.
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de Smet MD, Bitar G, Mainigi S, Nussenblatt RB. Human S-antigen determinant recognition in uveitis. Invest Ophthalmol Vis Sci. 2001 Dec; 42(13):3233-8.
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Vrabec TR. Exudative retinal detachment in Beh?et disease. Arch Ophthalmol. 2001 Sep; 119(9):1383-6.