"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 SyndromeEhlers-Danlos SyndromeEhlers Danlos SyndromeSyndrome, Ehlers-DanlosCutis ElasticaEhlers Danlos DiseaseDanlos Disease, EhlersDisease, Ehlers DanlosEhlers-Danlos DiseaseDisease, Ehlers-Danlos
 Ehlers-Danlos Syndrome, Type IVEhlers-Danlos Syndrome, Type IVEhlers Danlos Syndrome, Type IVEhlers-Danlos Syndrome, Arterial TypeEhlers-Danlos Syndrome, Ecchymotic TypeEhlers-Danlos Syndrome, Sack-Barabas TypeEhlers Danlos Syndrome, Sack-Barabas TypeEhlers Danlos Syndrome, Sack Barabas TypeEhlers-Danlos Syndrome, Type IV, Autosomal DominantEhlers Danlos Syndrome Type 4, Autosomal DominantEhlers Danlos Syndrome, Arterial TypeEhlers Danlos Syndrome, Ecchymotic TypeEhlers-Danlos Syndrome, Vascular TypeEhlers Danlos Syndrome, Vascular TypeEDS 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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		            | 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 | 
| 2014 | 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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								Mycotic aneurysm and fungal spinal abscess due to tainted steroid injection. Br J Neurosurg. 2014 Jun; 28(3):416-7. 
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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.