"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
|
| 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
|
| 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 |
|---|
| 1994 | 1 | 0 | 1 |
| 1996 | 1 | 0 | 1 |
| 1997 | 1 | 0 | 1 |
| 1998 | 1 | 0 | 1 |
| 1999 | 0 | 1 | 1 |
| 2000 | 1 | 0 | 1 |
| 2003 | 1 | 0 | 1 |
| 2011 | 2 | 0 | 2 |
| 2012 | 1 | 0 | 1 |
| 2013 | 1 | 1 | 2 |
| 2014 | 0 | 1 | 1 |
| 2016 | 0 | 1 | 1 |
| 2017 | 3 | 1 | 4 |
| 2018 | 2 | 0 | 2 |
| 2019 | 1 | 0 | 1 |
| 2020 | 3 | 0 | 3 |
| 2021 | 3 | 0 | 3 |
| 2022 | 3 | 0 | 3 |
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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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Evaluating perinatal and neonatal outcomes among children with vascular Ehlers-Danlos syndrome. Genet Med. 2022 10; 24(10):2134-2143.
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Cardiovascular Outcomes in Aortopathy: GenTAC Registry of Genetically Triggered Aortic Aneurysms and Related Conditions. J Am Coll Cardiol. 2022 05 31; 79(21):2069-2081.
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Molecular alterations due to Col5a1 haploinsufficiency in a mouse model of classic Ehlers-Danlos syndrome. Hum Mol Genet. 2022 04 22; 31(8):1325-1335.
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Sensing hand position in Ehlers-Danlos syndrome. Somatosens Mot Res. 2021 12; 38(4):303-314.
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Implications of Ehlers-Danlos Syndrome in a Patient With Mayer-Rokitansky-K?ster-Hauser Syndrome. J Pediatr Adolesc Gynecol. 2021 Dec; 34(6):890-892.
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Experience With Vertical Sleeve Gastrectomy in Adolescent and Young Adult Ehlers-Danlos Syndrome Patients: a Case Series and Review of the Literature. Obes Surg. 2021 09; 31(9):4168-4173.
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Intraperitoneal bladder rupture in a young child with vascular Ehlers-Danlos syndrome. Am J Med Genet A. 2021 03; 185(3):841-844.
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Ehlers-Danlos Syndrome: An Analysis of the Current Treatment Options. Pain Physician. 2020 07; 23(4):429-438.
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Setting a research agenda for vascular Ehlers-Danlos syndrome using a patient and stakeholder engagement model. J Vasc Surg. 2020 10; 72(4):1436-1444.e2.
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Gynecologic Management of Pediatric and Adolescent Patients with Ehlers-Danlos Syndrome. J Pediatr Adolesc Gynecol. 2020 Jun; 33(3):291-295.