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: 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.)
- Ehlers-Danlos Syndrome Hypermobility Type (Marfan Foundation) - PDF
- Genetics Home Reference: Ehlers-Danlos syndrome (National Library of Medicine)
- ClinicalTrials.gov: Ehlers-Danlos Syndrome (National Institutes of Health)
Journal ArticlesReferences and abstracts from MEDLINE/PubMed (National Library of Medicine)
- Article: A 19-year-old man with relapsing bilateral pneumothorax, hemoptysis, and intrapulmonary...
- Article: Brittle cornea syndrome ZNF469 mutation carrier phenotype and segregation analysis...
- Article: Vascular Ehlers-Danlos syndrome without the characteristic facial features: a case...
- Ehlers-Danlos Syndrome -- see more articles