Behcet Syndrome

"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.

MeSH information

Definition | Details | More General Concepts | Related Concepts | More Specific Concepts

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".

Diseases [C]
Stomatognathic Diseases [C07]
Mouth Diseases [C07.465]
Behcet Syndrome [C07.465.075]
Eye Diseases [C11]
Uveal Diseases [C11.941]
Uveitis [C11.941.879]
Panuveitis [C11.941.879.780]
Uveitis, Anterior [C11.941.879.780.880]
Behcet Syndrome [C11.941.879.780.880.200]
Cardiovascular Diseases [C14]
Vascular Diseases [C14.907]
Vasculitis [C14.907.940]
Behcet Syndrome [C14.907.940.100]
Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]
Genetic Diseases, Inborn [C16.320]
Hereditary Autoinflammatory Diseases [C16.320.382]
Behcet Syndrome [C16.320.382.250]
Skin and Connective Tissue Diseases [C17]
Skin Diseases [C17.800]
Skin Diseases, Genetic [C17.800.827]
Hereditary Autoinflammatory Diseases [C17.800.827.368]
Behcet Syndrome [C17.800.827.368.250]
Skin Diseases, Vascular [C17.800.862]
Behcet Syndrome [C17.800.862.150]

Below are MeSH descriptors whose meaning is related to "Behcet Syndrome".

Below are MeSH descriptors whose meaning is more specific than "Behcet Syndrome".

publications

Timeline | Most Recent

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.

Bar chart showing 10 publications over 6 distinct years, with a maximum of 2 publications in 2014 and 2015 and 2019 and 2021

To see the data from this visualization as text, click here.

Year	Major Topic	Minor Topic	Total
2005	0	1	1
2010	1	0	1
2014	2	0	2
2015	2	0	2
2019	2	0	2
2021	2	0	2

Below are the most recent publications written about "Behcet Syndrome" by people in Profiles.

Jiang W, Deng M, Gan C, Wang L, Mao H, Li Q. A novel missense mutation in TNFAIP3 causes haploinsufficiency of A20. Cell Immunol. 2022 01; 371:104453.

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Wilkins CS, Goduni L, Dedania VS, Modi YS, Johnson B, Mehta N, Weng CY. Diagnostic and Therapeutic Challenge. Retina. 2021 Jul 01; 41(7):1570-1576.

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Suryavanshi SV, Li N. Behçet's disease: A (silk) route to atrial fibrillation? Int J Cardiol. 2019 10 15; 293:117-118.

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Oezguen N, Yalcinkaya N, Kücükali CI, Dahdouli M, Hollister EB, Luna RA, Türkoglu R, Kürtüncü M, Eraksoy M, Savidge TC, Tüzün E. Microbiota stratification identifies disease-specific alterations in neuro-Behçet's disease and multiple sclerosis. Clin Exp Rheumatol. 2019 Nov-Dec; 37 Suppl 121(6):58-66.

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Rottenstreich A, Machol K, Eisenstein EM, Padeh S, Klar A, Livneh A, Berkun Y. Behçet'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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Morgan ML, Espino Barros Palau A, Lee AG, Foroozan R. Neuro-Behçet disease presenting with oculopalatal tremor. J Neuroophthalmol. 2015 Mar; 35(1):51-3.

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Hede SV, Morales DL, Parekh DR. At the heart of the old silk road. J Gen Intern Med. 2014 Oct; 29(10):1421-2.

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Rao S, Rao S, Dhindsa-Castanedo L, Benndorf G. Rapidly evolving large extracranial vertebral artery pseudoaneurysm in Behçet's disease: Case report and review of the literature. Mod Rheumatol. 2015 May; 25(3):476-9.

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Remmers EF, Cosan F, Kirino Y, Ombrello MJ, Abaci N, Satorius C, Le JM, Yang B, Korman BD, Cakiris A, Aglar O, Emrence Z, Azakli H, Ustek D, Tugal-Tutkun I, Akman-Demir G, Chen W, Amos CI, Dizon MB, Kose AA, Azizlerli G, Erer B, Brand OJ, Kaklamani VG, Kaklamanis P, Ben-Chetrit E, Stanford M, Fortune F, Ghabra M, Ollier WE, Cho YH, Bang D, O'Shea J, Wallace GR, Gadina M, Kastner DL, Gül A. Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behçet's disease. Nat Genet. 2010 Aug; 42(8):698-702.

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Alrefai A, El-Salem K, Saadeh R, Al-Balas H. A case report of cranial polyneuropathy in Behcet's disease. Neurol Sci. 2010 Feb; 31(1):83-5.

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