"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
|
| 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
|
| Concept/Terms |
Marfan Syndrome- Marfan Syndrome
- Syndrome, Marfan
- Marfan Syndrome, Type I
- Marfan's Syndrome
- Marfans Syndrome
- Syndrome, Marfan's
|
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 |
|---|
| 1999 | 1 | 0 | 1 |
| 2004 | 1 | 0 | 1 |
| 2005 | 4 | 1 | 5 |
| 2007 | 2 | 1 | 3 |
| 2008 | 1 | 1 | 2 |
| 2009 | 1 | 0 | 1 |
| 2010 | 1 | 0 | 1 |
| 2011 | 1 | 1 | 2 |
| 2014 | 2 | 0 | 2 |
| 2015 | 1 | 0 | 1 |
| 2016 | 1 | 0 | 1 |
| 2018 | 0 | 1 | 1 |
| 2019 | 0 | 1 | 1 |
| 2020 | 1 | 0 | 1 |
| 2023 | 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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Prevalence and Complications of Aberrant Subclavian Artery in Patients With Heritable and Nonheritable Arteriopathies. J Am Coll Cardiol. 2023 03 14; 81(10):979-991.
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Aortic root dilation in a child with Marfan syndrome and mosaic Turner syndrome. Cardiol Young. 2020 Dec; 30(12):1976-1977.
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Ulnar Artery Aneurysm as a Late Sequela of Marfan Syndrome. J Hand Surg Am. 2020 Nov; 45(11):1090.e1-1090.e5.
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Management of the aortic arch in patients with Loeys-Dietz syndrome. J Thorac Cardiovasc Surg. 2020 Nov; 160(5):1166-1175.
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Valve-sparing aortic root replacement in children: Outcomes from 100 consecutive cases. J Thorac Cardiovasc Surg. 2019 03; 157(3):1100-1109.
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Recurrent spontaneous scleral rupture in Marfan's syndrome. BMJ Case Rep. 2016 May 19; 2016.
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Palliative Mitral Valve Repair During Infancy for Neonatal Marfan Syndrome. Ann Thorac Surg. 2016 May; 101(5):1987-8.
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Long-term outcomes of aortic root operations for Marfan syndrome: A comparison of Bentall versus aortic valve-sparing procedures. J Thorac Cardiovasc Surg. 2016 Feb; 151(2):330-6.
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Management of the pregnant woman with Marfan syndrome complicated by ascending aorta dilation. Arch Gynecol Obstet. 2014 Oct; 290(4):797-802.
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Early and 1-year outcomes of aortic root surgery in patients with Marfan syndrome: a prospective, multicenter, comparative study. J Thorac Cardiovasc Surg. 2014 Jun; 147(6):1758-66, 1767.e1-4.