"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.
To see the data from this visualization as text,
click here.
| Year | Major Topic | Minor Topic | Total |
|---|
| 2005 | 0 | 1 | 1 |
| 2013 | 1 | 0 | 1 |
| 2016 | 0 | 1 | 1 |
| 2022 | 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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Holmes KW, Markwardt S, Eagle KA, Devereux RB, Weinsaft JW, Asch FM, LeMaire SA, Maslen CL, Song HK, Milewicz DM, Prakash SK, Guo D, Morris SA, Pyeritz RE, Milewski RC, Ravekes WJ, Dietz HC, Shohet RV, Silberbach M, Roman MJ. 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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Weinsaft JW, Devereux RB, Preiss LR, Feher A, Roman MJ, Basson CT, Geevarghese A, Ravekes W, Dietz HC, Holmes K, Habashi J, Pyeritz RE, Bavaria J, Milewski K, LeMaire SA, Morris S, Milewicz DM, Prakash S, Maslen C, Song HK, Silberbach GM, Shohet RV, McDonnell N, Hendershot T, Eagle KA, Asch FM. Aortic Dissection in Patients With Genetically Mediated Aneurysms: Incidence and Predictors in the GenTAC Registry. J Am Coll Cardiol. 2016 06 14; 67(23):2744-2754.
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Jim?nez-Encarnaci?n E, Vil? LM. Recurrent venous thrombosis in Ehlers-Danlos syndrome type III: an atypical manifestation. BMJ Case Rep. 2013 Jun 27; 2013.
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Sollecito TP, Sullivan KE, Pinto A, Stewart J, Korostoff J. Systemic conditions associated with periodontitis in childhood and adolescence. A review of diagnostic possibilities. Med Oral Patol Oral Cir Bucal. 2005 Mar-Apr; 10(2):142-50.