"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 | 
|---|
| 1996 | 1 | 0 | 1 | 
| 2005 | 1 | 0 | 1 | 
| 2010 | 0 | 1 | 1 | 
| 2020 | 1 | 0 | 1 | 
| 2021 | 1 | 0 | 1 | 
| 2023 | 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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								Sensory Profiling in Classical Ehlers-Danlos Syndrome: A Case-Control Study Revealing Pain Characteristics, Somatosensory Changes, and Impaired Pain Modulation. J Pain. 2023 11; 24(11):2063-2078. 
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								Pain in the Ehlers-Danlos syndromes: Mechanisms, models, and challenges. Am J Med Genet C Semin Med Genet. 2021 12; 187(4):429-445. 
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								Pain-related behaviors and abnormal cutaneous innervation in a murine model of classical Ehlers-Danlos syndrome. Pain. 2020 10; 161(10):2274-2283. 
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								Patellofemoral instability in athletes: treatment via modified Fulkerson osteotomy and lateral release. Am J Sports Med. 2010 May; 38(5):992-9. 
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								Filamin A mutations cause periventricular heterotopia with Ehlers-Danlos syndrome. Neurology. 2005 Jan 25; 64(2):254-62. 
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								Fatal vascular catastrophe in Ehlers-Danlos syndrome: a case report and review. J Emerg Med. 1996 Jan-Feb; 14(1):25-31.