 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 |
|---|
| 1983 | 1 | 0 | 1 | | 1985 | 0 | 1 | 1 | | 1993 | 1 | 0 | 1 | | 2004 | 0 | 1 | 1 | | 2011 | 0 | 1 | 1 | | 2014 | 2 | 0 | 2 |
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Below are the most recent publications written about "Marfan Syndrome" by people in Profiles.
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Lally DR, Monsonego J. Images in clinical medicine. Ectopia lentis in Marfan's syndrome. N Engl J Med. 2014 Nov 06; 371(19):e28.
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Paraskos JA. Systemic inflammatory response following transcatheter aortic valve implantation. Cardiology. 2014; 128(1):13-4.
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Trimarchi S, Jonker FH, Hutchison S, Isselbacher EM, Pape LA, Patel HJ, Froehlich JB, Muhs BE, Rampoldi V, Grassi V, Evangelista A, Meinhardt G, Beckman J, Myrmel T, Pyeritz RE, Hirsch AT, Sundt TM, Nienaber CA, Eagle KA. Descending aortic diameter of 5.5 cm or greater is not an accurate predictor of acute type B aortic dissection. J Thorac Cardiovasc Surg. 2011 Sep; 142(3):e101-7.
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Januzzi JL, Isselbacher EM, Fattori R, Cooper JV, Smith DE, Fang J, Eagle KA, Mehta RH, Nienaber CA, Pape LA. Characterizing the young patient with aortic dissection: results from the International Registry of Aortic Dissection (IRAD). J Am Coll Cardiol. 2004 Feb 18; 43(4):665-9.
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Gordon CF, Johnson MD. Anesthetic management of the pregnant patient with Marfan syndrome. J Clin Anesth. 1993 May-Jun; 5(3):248-51.
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Barter SJ, Hicks IP, Hartnell GG, Leung AW. Nuclear magnetic resonance imaging in the assessment of unusual abdominal aortic aneurysms. Clin Radiol. 1985 Jul; 36(4):419-22.
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Manning GS, Stevens KA, Stock JL. Multiple endocrine neoplasia, type I. Association with marfanoid habitus, optic atrophy, and other abnormalities. Arch Intern Med. 1983 Dec; 143(12):2315-6.
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