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.
- Ehlers-Danlos syndrome Available in Spanish
- Ehlers-Danlos Syndrome (Mayo Foundation for Medical Education and Research)
- Ehlers-Danlos Syndrome Hypermobility Type (Marfan Foundation) - PDF
- Ehlers-Danlos Syndrome: Causes and Symptoms (Ehlers-Danlos Syndrome Network C.A.R.E.S.)
- Ehlers-Danlos Syndrome: Myths and Facts (Ehlers-Danlos Syndrome Network C.A.R.E.S.)
- Genetics Home Reference: Ehlers-Danlos syndrome (National Library of Medicine)
- Heritable Disorders of Connective Tissue (National Institute of Arthritis and Musculoskeletal and Skin Diseases)
- ClinicalTrials.gov: Ehlers-Danlos Syndrome (National Institutes of Health)