EDS Today Information and support to people living with EDS, their families, and the medical community.
Ehlers-Danlos Syndrome Foundation The Ehlers-Danlos National Foundation (EDNF) was created in 1985 by Nancy Hanna Rogowski. The primary goal of EDNF is to provide emotional support and updated information to those affected by Ehlers-Danlos syndrome and to their family members.
Family Village -- Ehlers-Danlos Syndrome Who to Contact Where to Go to Chat with Others Learn More About It Web Sites Search AltaVista for "Ehlers-Danlos Syndrome" Who to Contact Ehlers-Danlos National Foundation (EDNF) 6399 Wilshire Boulevard, Suite 510 Los Angeles
Kathy's Page - Ehlers-Danlos Syndrome Ehlers-Danlos Syndrome (EDS) is a heterogeneous group of heritable connective tissue disorders, characterized by articular (joint) hypermobility, skin extensibility and tissue fragility.
The Ehlers Danlos Syndrome The Ehlers-Danlos Syndrome (EDS) is a group of genetic conditions that have resulted from defects in a collagen molecule which would normally give strength and adhesion to the body's tissues. In many cases the disorder affects the skin and it can become excessively extendible (stretchy), fragile and bruise easily.
Vanderbuilt Medical Center-Ehlers-Danlos syndrome, aka Cutis Laxa. Presents an easy to understand report on the symptoms and causes of Ehlers-Danlos syndromes (EDS) comprise a heterogenous group of connective tissue disorders that share, as fundamental features, alterations of the integrity of the supporting structures of the body and inheritance in a simple Mendelian fashion