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Ehlers-Danlos Syndrome (EDS)

What Is It?
What Are the Symptoms?
How Is It Diagnosed?
Treatment Options
Resources and Suggestions

What Is It?

Ehlers-Danlos Syndrome (A-lerz-DAN-los SIN-drome) describes a group of hereditary disorders which mainly affect the skin and joints, but may affect other organs. EDS affects the connective tissues -- the tissues that support various parts of the body such as skin, muscles, tendons and ligaments. In EDS, the fibrous protein collagen is faulty, causing the connective tissue to not be elastic or strong.

What Are the Symptoms?

There are 9 types of EDS and symptoms differ depending on the type of EDS. Type I and III have the following:

  • Skin problems, include fragile skin that bruises or tears; soft skin, and slow-healing wounds.
  • Joint problems, including loose, unstable joints; "double-jointed" or overextension of the joints; arthritis-like problems.

Other types may have these symptoms:

  • Lung problems; weak blood vessels; eye problems; curvature of the spine; gum diseases; problems with blood clotting.

How Is It Diagnosed?

  • A review of family and medical history.
  • Physical exam, checking for joint overextension.
  • Skin biopsy may be performed to study chemical makeup of connective tissue.

Treatment Options

  • Diet - to reduce weight
  • Vitamin C
  • Exercise
  • Eye treatments
  • Joint protection
  • Protection from the sun
  • Surgery to correct fractures or dislocated joints

Resources and Suggestions

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