URL of this page: http://www.nlm.nih.gov/medlineplus/ehlersdanlossyndrome.html

Ehlers-Danlos Syndrome

Also called: Cutis elastica, EDS 
On this page

Multimedia & Tools

  • No links available

Reference Shelf

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.

Start Here

Diagnosis/Symptoms

Specific Conditions

Related Issues

Clinical Trials

Genetics

Patient Handouts