Ehlers-Danlos Syndrome.

Diagnosis and evaluation

How is ehlers-danlos syndrome diagnosed?

Specific diagnostic tests are available for some types of EDS in which there is a known biochemical defect. Doctors will also review your family and medical histories and perform a complete physical examination.

Having EDS is more than being limber or double-jointed. "Over extension" is the ability to flex the joints beyond normal limits.

Sometimes, a skin biopsy may be performed to study the chemical make-up of the connective tissue. (A biopsy is a simple, almost painless procedure in which a tiny piece of skin is removed for examination in the laboratory.).

What health care professionals may help diagnose ehlers-danlos syndrome?

Because Ehlers-Danlos is uncommon, it is important to find a doctor who has experience with its diagnosis and treatment. Many family doctors, pediatricians, arthritis specialists, skin specialists and specialists in medical genetics are able to diagnose and/or treat Ehlers-Danlos syndrome. If you are unable to find a knowledgeable doctor in your area, contact the Ehlers-Danlos National Foundation.

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