Ehlers-Danlos syndrome is a group of inherited disorders marked by extremely loose joints, hyperelastic skin that bruises easily, and easily damaged blood vessels.
There are six major types of Ehlers-Danlos syndrome (EDS). A variety of different gene problems cause problems with collagen, the material that provides strength and structure to skin and bone tissue, blood vessels, and internal organs. (The syndrome sometimes involves rupture of internal organs.) Family history is a risk factor in some cases.
Examination by the health care provider may show: Tests:
There is no specific cure for Ehlers-Danlos syndrome, so individual problems and symptoms must be evaluated and cared for appropriately. Frequently, physical therapy or evaluation by a physician specializing in rehabilitation medicine is needed.
People with EDS generally have a normal life span. Intelligence is normal. Patients with the rare vascular type of EDS are at significantly increased risk for rupture of a major organ or blood vessel. These patients therefore have a high risk of sudden death.
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Reviewer Info: Brian Kirmse, MD, Mount Sinai School of Medicine, Department of Human Genetics, New York, NY. Review provided by VeriMed Healthcare Network.; ADAM Health Illustrated Encyclopedia, 12/11/2006 |