"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
|
| 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,
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| Year | Major Topic | Minor Topic | Total |
|---|
| 2005 | 0 | 1 | 1 |
| 2010 | 1 | 0 | 1 |
| 2014 | 2 | 0 | 2 |
| 2015 | 3 | 0 | 3 |
| 2017 | 1 | 0 | 1 |
| 2019 | 2 | 0 | 2 |
| 2021 | 2 | 0 | 2 |
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click here.
Below are the most recent publications written about "Behcet Syndrome" by people in Profiles.
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Clinical, Endoscopic, and Histopathologic Gastrointestinal Disease in an American Cohort With Beh?et's Disease. Clin Transl Gastroenterol. 2023 08 01; 14(8):e00591.
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A novel missense mutation in TNFAIP3 causes haploinsufficiency of A20. Cell Immunol. 2022 01; 371:104453.
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Diagnostic and Therapeutic Challenge. Retina. 2021 Jul 01; 41(7):1570-1576.
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Beh?et's disease: A (silk) route to atrial fibrillation? Int J Cardiol. 2019 10 15; 293:117-118.
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Microbiota stratification identifies disease-specific alterations in neuro-Beh?et's disease and multiple sclerosis. Clin Exp Rheumatol. 2019 Nov-Dec; 37 Suppl 121(6):58-66.
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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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Beh?et's disease and cerebral sinus vein thrombosis in children: a case study and review of the literature. Clin Exp Rheumatol. 2015 Nov-Dec; 33(6 Suppl 94):S163-8.
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Gastrointestinal Beh?et's disease: a review. World J Gastroenterol. 2015 Apr 07; 21(13):3801-12.
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Neuro-Beh?et disease presenting with oculopalatal tremor. J Neuroophthalmol. 2015 Mar; 35(1):51-3.
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At the heart of the old silk road. J Gen Intern Med. 2014 Oct; 29(10):1421-2.