 Marfan Syndrome
"Marfan 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.
An autosomal dominant disorder of CONNECTIVE TISSUE with abnormal features in the heart, the eye, and the skeleton. Cardiovascular manifestations include MITRAL VALVE PROLAPSE, dilation of the AORTA, and aortic dissection. Other features include lens displacement (ectopia lentis), disproportioned long limbs and enlarged DURA MATER (dural ectasia). Marfan syndrome is associated with mutations in the gene encoding fibrillin, a major element of extracellular microfibrils of connective tissue.
| Descriptor ID |
D008382
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| MeSH Number(s) |
C05.116.099.674 C14.240.400.725 C14.280.400.725 C16.131.077.550 C16.131.240.400.720 C16.320.540 C17.300.500
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| Concept/Terms |
Marfan Syndrome- Marfan Syndrome
- Syndrome, Marfan
- Marfan Syndrome, Type I
- Marfan's Syndrome
- Marfans Syndrome
- Syndrome, Marfan's
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Below are MeSH descriptors whose meaning is more general than "Marfan Syndrome".
Below are MeSH descriptors whose meaning is more specific than "Marfan Syndrome".
This graph shows the total number of publications written about "Marfan Syndrome" by people in this website by year, and whether "Marfan 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 |
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| 2005 | 1 | 0 | 1 | | 2006 | 1 | 0 | 1 | | 2009 | 2 | 0 | 2 | | 2011 | 1 | 0 | 1 | | 2012 | 1 | 0 | 1 | | 2013 | 0 | 1 | 1 | | 2014 | 1 | 0 | 1 | | 2016 | 1 | 3 | 4 | | 2017 | 1 | 2 | 3 | | 2018 | 1 | 0 | 1 | | 2019 | 1 | 1 | 2 | | 2020 | 1 | 0 | 1 | | 2021 | 1 | 0 | 1 |
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Below are the most recent publications written about "Marfan Syndrome" by people in Profiles.
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Ricceri SK, Bang TJ, Goodwin A, Khanna A, Groves DW, Kollengode MS. Coronary artery complications related to aortic root replacement in Marfan syndrome. J Cardiovasc Comput Tomogr. 2022 Jan-Feb; 16(1):e5-e7.
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Tcheandjieu C, Aguirre M, Gustafsson S, Saha P, Potiny P, Haendel M, Ingelsson E, Rivas MA, Priest JR. A phenome-wide association study of 26 mendelian genes reveals phenotypic expressivity of common and rare variants within the general population. PLoS Genet. 2020 11; 16(11):e1008802.
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Kim AJ, Xu N, Umeyama K, Hulin A, Ponny SR, Vagnozzi RJ, Green EA, Hanson P, McManus BM, Nagashima H, Yutzey KE. Deficiency of Circulating Monocytes Ameliorates the Progression of Myxomatous Valve Degeneration in Marfan Syndrome. Circulation. 2020 01 14; 141(2):132-146.
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Khanna AD, Duca LM, Kay JD, Shore J, Kelly SL, Crume T. Prevalence of Mental Illness in Adolescents and Adults With Congenital Heart Disease from the Colorado Congenital Heart Defect Surveillance System. Am J Cardiol. 2019 08 15; 124(4):618-626.
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Lindeman JH, Matsumura JS. Pharmacologic Management of Aneurysms. Circ Res. 2019 02 15; 124(4):631-646.
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Sch?fer M, Browne LP, Truong U, Jaggers JJ, Mitchell MB, Malone L, Morgan G, Chatfield K, McLennan D, Turbendian H, Vargas D, Fonseca B, DiMaria M, Shah A, Ivy MP, Barker AJ, Hunter KS, Wilson N, Ivy DD, Campbell DN. Aortic stiffness in adolescent Turner and Marfan syndrome patients. Eur J Cardiothorac Surg. 2018 11 01; 54(5):926-932.
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Ikeno Y, Yokawa K, Nakai H, Yamanaka K, Inoue T, Tanaka H, Okita Y. Results of staged repair of aortic disease in patients with Marfan syndrome. J Thorac Cardiovasc Surg. 2019 06; 157(6):2138-2147.e2.
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Rao P, Keenan JB, Rajab TK, Kim S, Smith R, Amabile O, Khalpey Z. Total artificial heart implantation in a young Marfan syndrome patient. Int J Artif Organs. 2018 Mar; 41(3):175-177.
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Dietl CA, Langsfeld M, S?nchez AM, Samedi VG. Hybrid reconstruction of the aortic arch: A 15-year follow-up. J Thorac Cardiovasc Surg. 2017 12; 154(6):e95-e97.
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D'Souza RS, Slavov D, Graw S, Jirikowic J, Todd E, Rogers RK, Taylor MR. Clinical and genetic characterization of adult patients presenting with non-syndromic vascular aneurysms and dissections. Int Angiol. 2017 Oct; 36(5):417-427.
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