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A Genetic Connective Tissue Disorder
What is
Ehlers-Danlos Syndrome?
This page was last updated: April 23, 2013
The Ehlers-Danlos syndromes are inherited in the genes that are passed from parents to offspring. They are categorized according to the form of genetic transmission into different types with many features differing between patients in any given type. The fragile skin and loose joints  and tissue fragility is often a result of abnormal genes that produce abnormal proteins that confer an inherited frailty of collagen (the normal protein "glue" of our tissues).

In 2001, researchers discovered a new form of Ehlers-Danlos syndrome that is caused by an inherited abnormality in a protein other than collagen that also normally plays a role in binding together the cells of our tissues (including the skin, tendons, muscle, and blood vessels). Abnormalities in this protein, called tenascin, also lead to a form of Ehlers-Danlos syndrome. Researchers suspect that tenascin could play a role in regulating the normal distribution of collagen in the connective tissues of the body.




Dr.. Diana Milewicz, MD, PhD

Lynn Sanders/President of
EDS Network C.A.R.E.S. Foundation

Dr. Amy Reid, MD
PhD Student
EDS Network C.A.R.E.S. Foundation
EDS Research
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Ehlers-Danlos Syndrome
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