"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
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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.
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click here.
| Year | Major Topic | Minor Topic | Total |
|---|
| 2005 | 0 | 1 | 1 |
| 2011 | 0 | 1 | 1 |
| 2012 | 1 | 0 | 1 |
| 2015 | 0 | 1 | 1 |
| 2023 | 1 | 0 | 1 |
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click here.
Below are the most recent publications written about "Ehlers-Danlos Syndrome" by people in Profiles.
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McElroy A, Gray-Edwards H, Coghill LM, Lyons LA. Precision medicine using whole genome sequencing in a cat identifies a novel COL5A1 variant for classical Ehlers-Danlos syndrome. J Vet Intern Med. 2023 Sep-Oct; 37(5):1716-1724.
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Riascos R, Bonfante E, Cotes C, Guirguis M, Hakimelahi R, West C. Imaging of Atlanto-Occipital and Atlantoaxial Traumatic Injuries: What the Radiologist Needs to Know. Radiographics. 2015 Nov-Dec; 35(7):2121-34.
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Abayazeed A, Hayman E, Moghadamfalahi M, Cain D. Vascular type Ehlers-Danlos Syndrome with fatal spontaneous rupture of a right common iliac artery dissection: case report and review of literature. J Radiol Case Rep. 2014 Feb; 8(2):63-9.
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Jeong SJ, Li S, Luo R, Strokes N, Piao X. Loss of Col3a1, the gene for Ehlers-Danlos syndrome type IV, results in neocortical dyslamination. PLoS One. 2012; 7(1):e29767.
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Calmus ML, Macksoud EE, Tucker R, Iozzo RV, Lechner BE. A mouse model of spontaneous preterm birth based on the genetic ablation of biglycan and decorin. Reproduction. 2011 Jul; 142(1):183-94.
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Maron BJ, Ackerman MJ, Nishimura RA, Pyeritz RE, Towbin JA, Udelson JE. Task Force 4: HCM and other cardiomyopathies, mitral valve prolapse, myocarditis, and Marfan syndrome. J Am Coll Cardiol. 2005 Apr 19; 45(8):1340-5.