"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.
View timeline visualization
| Year | Major Topic | Minor Topic | Total |
|---|
| 1996 | 1 | 0 | 1 |
| 1997 | 1 | 0 | 1 |
| 1998 | 2 | 0 | 2 |
| 2000 | 1 | 0 | 1 |
| 2001 | 2 | 0 | 2 |
| 2006 | 1 | 1 | 2 |
| 2008 | 2 | 0 | 2 |
| 2009 | 0 | 3 | 3 |
| 2011 | 1 | 0 | 1 |
| 2012 | 1 | 0 | 1 |
| 2013 | 2 | 0 | 2 |
| 2015 | 4 | 0 | 4 |
| 2016 | 1 | 0 | 1 |
| 2017 | 1 | 1 | 2 |
| 2019 | 2 | 2 | 4 |
| 2020 | 1 | 0 | 1 |
| 2021 | 4 | 0 | 4 |
| 2022 | 1 | 0 | 1 |
| 2023 | 1 | 0 | 1 |
| 2024 | 2 | 0 | 2 |
Below are the most recent publications written about "Behcet Syndrome" by people in Profiles.
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Dyspnea Investigation in Behçet's Disease: The Role of Advanced Diagnostic Methods to Elucidate Dyspnea in Systemic Diseases. Ann Am Thorac Soc. 2024 Jun; 21(6):977-982.
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The Complexity of Being A20: From Biological Functions to Genetic Associations. J Clin Immunol. 2024 03 07; 44(3):76.
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Cardiovascular risk in vasculitis. Best Pract Res Clin Rheumatol. 2023 03; 37(1):101831.
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The role of bacteria and viruses in Behçet syndrome: Should we move towards new paradigms? Autoimmun Rev. 2023 Feb; 22(2):103237.
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Behcet's Disease Mimicking Crohn's Disease: A Diagnostic Pitfall in GI Tract Biopsies. Int J Surg Pathol. 2023 Aug; 31(5):606-611.
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A prospective observational cohort study and systematic review of 40 patients with mouth and genital ulcers with inflamed cartilage (MAGIC) syndrome. Semin Arthritis Rheum. 2022 02; 52:151924.
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Epidemiology and treatment of Behçet's disease in the USA: insights from the Rheumatology Informatics System for Effectiveness (RISE) Registry with a comparison with other published cohorts from endemic regions. Arthritis Res Ther. 2021 08 30; 23(1):224.
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Three-dimensional cardiac print assisted percutaneous closure of left ventricular pseudoaneurysm in patient with Behçet's disease. Catheter Cardiovasc Interv. 2022 02; 99(2):512-517.
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Behçet disease, new insights in disease associations and manifestations: a next-generation sequencing study. Clin Exp Immunol. 2021 04; 204(1):144-151.
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Premature coronary disease, in-stent restenosis and vascular complications in a young man with Behçet syndrome. BMJ Case Rep. 2020 Aug 24; 13(8).