"Ehlers-Danlos 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.
A heterogeneous group of autosomally inherited COLLAGEN DISEASES caused by defects in the synthesis or structure of FIBRILLAR COLLAGEN. There are numerous subtypes: classical, hypermobility, vascular, and others. Common clinical features include hyperextensible skin and joints, skin fragility and reduced wound healing capability.
| Descriptor ID |
D004535
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| MeSH Number(s) |
C14.907.454.240 C15.378.463.515.240 C16.131.831.428 C16.320.850.260 C17.300.200.310 C17.800.804.428 C17.800.827.260
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| Concept/Terms |
Ehlers-Danlos Syndrome- Ehlers-Danlos Syndrome
- Ehlers Danlos Syndrome
- Syndrome, Ehlers-Danlos
- Cutis Elastica
- Ehlers Danlos Disease
- Danlos Disease, Ehlers
- Disease, Ehlers Danlos
- Ehlers-Danlos Disease
- Disease, Ehlers-Danlos
Ehlers-Danlos Syndrome, Type IV- Ehlers-Danlos Syndrome, Type IV
- Ehlers Danlos Syndrome, Type IV
- Ehlers-Danlos Syndrome, Arterial Type
- Ehlers-Danlos Syndrome, Ecchymotic Type
- Ehlers-Danlos Syndrome, Sack-Barabas Type
- Ehlers Danlos Syndrome, Sack-Barabas Type
- Ehlers Danlos Syndrome, Sack Barabas Type
- Ehlers-Danlos Syndrome, Type IV, Autosomal Dominant
- Ehlers Danlos Syndrome Type 4, Autosomal Dominant
- Ehlers Danlos Syndrome, Arterial Type
- Ehlers Danlos Syndrome, Ecchymotic Type
- Ehlers-Danlos Syndrome, Vascular Type
- Ehlers Danlos Syndrome, Vascular Type
- EDS IV
|
Below are MeSH descriptors whose meaning is more general than "Ehlers-Danlos Syndrome".
Below are MeSH descriptors whose meaning is more specific than "Ehlers-Danlos Syndrome".
This graph shows the total number of publications written about "Ehlers-Danlos Syndrome" by people in this website by year, and whether "Ehlers-Danlos 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 |
|---|
| 1998 | 1 | 0 | 1 |
| 2005 | 0 | 1 | 1 |
| 2006 | 0 | 1 | 1 |
| 2008 | 0 | 1 | 1 |
| 2011 | 0 | 1 | 1 |
| 2017 | 2 | 0 | 2 |
| 2019 | 1 | 0 | 1 |
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Below are the most recent publications written about "Ehlers-Danlos Syndrome" by people in Profiles.
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Keeping a Flexible Differential Diagnosis: an Exercise in Clinical Reasoning. J Gen Intern Med. 2019 06; 34(6):1063-1068.
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Spectrum of mucocutaneous, ocular and facial features and delineation of novel presentations in 62 classical Ehlers-Danlos syndrome patients. Clin Genet. 2017 Dec; 92(6):624-631.
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Revision pediatric anterior cruciate ligament reconstruction after failure of iliotibial band technique treated with all-epiphyseal technique in a prepubescent with Ehlers-Danlos syndrome: a case report. J Pediatr Orthop B. 2017 Sep; 26(5):470-476.
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Arthroscopic ligamentum teres reconstruction of the hip in Ehlers-Danlos syndrome: a case study. Hip Int. 2015 May-Jun; 25(3):286-91.
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Liver transplantation in a patient with Ehlers-Danlos syndrome. Liver Transpl. 2013 May; 19(5):565-6.
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Tenascin-X haploinsufficiency associated with Ehlers-Danlos syndrome in patients with congenital adrenal hyperplasia. J Clin Endocrinol Metab. 2013 Feb; 98(2):E379-87.
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Impact of joint laxity and hypermobility on the musculoskeletal system. J Am Acad Orthop Surg. 2011 Aug; 19(8):463-71.
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Thoracic aortic aneurysm syndrome in children. Semin Thorac Cardiovasc Surg Pediatr Card Surg Annu. 2008; 11-21.
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Periventricular heterotopia: phenotypic heterogeneity and correlation with Filamin A mutations. Brain. 2006 Jul; 129(Pt 7):1892-906.
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Limited role of aortic size in the genesis of acute type A aortic dissection. Eur J Cardiothorac Surg. 2005 Dec; 28(6):857-63.