Summary
Ehlers-Danlos syndrome (EDS) is a group of inherited disorders that weaken connective tissues. Connective tissues are proteins that support skin, bones, blood vessels, and other organs.
EDS usually affects your skin, joints and blood vessel walls. Symptoms include:
- Loose joints
- Fragile, small blood vessels
- Abnormal scar formation and wound healing
- Soft, velvety, stretchy skin that bruises easily
There are several types of EDS. They can range from mild to life-threatening. About 1 in 5,000 people has EDS. There is no cure. Treatment involves managing symptoms, often with medicines and physical therapy. It also includes learning how to protect your joints and prevent injuries.
Learn More
- Ehlers-Danlos syndrome (Medical Encyclopedia) Also in Spanish
- Ehlers-Danlos Syndrome (Mayo Foundation for Medical Education and Research)
- Ehlers-Danlos Syndrome Hypermobility Type (Marfan Foundation) - PDF
Genetics
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Ehlers-Danlos syndrome: MedlinePlus Genetics
(National Library of Medicine)
Clinical Trials
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ClinicalTrials.gov: Ehlers-Danlos Syndrome
(National Institutes of Health)
Journal Articles References and abstracts from MEDLINE/PubMed (National Library of Medicine)
- Article: Hypermobile Ehlers Danlos for the Primary Care Provider.
- Article: A machine learning approach to stratify patients with hypermobile Ehlers-Danlos syndrome/hypermobility...
- Article: Exploring signs of central sensitization in adolescents with hypermobility Spectrum disorder...
- Ehlers-Danlos Syndrome -- see more articles
Find an Expert
- Find a Genetic Counselor (National Society of Genetic Counselors)