Learn more about how Ehlers-Danlos Syndrome is identified, diagnosed and treated.
EHLERS-DANLOS INFORMATION PAGE (PDF)
Ehlers-Danlos Syndrome (EDS) is a hereditary connective tissue disorder. It is caused by genetic changes that affect the connective tissue that stabilize and support the joints and organs throughout the body.
There are many different types of EDS, including the following:
Some common symptoms for EDS may include:
The best way to get a diagnosis of Ehlers-Danlos syndrome is to see a clinical geneticist, but first, a comprehensive clinical evaluation and full medical history is required.
Ehlers-Danlos syndrome Type III is the most common. It is the hypermobile type. Usually, this type of Ehlers-Danlos syndrome is diagnosed either by a geneticist familiar with this type, or in the clinic using what doctors called the Beighton Score/Scale.
You can learn more about this score here: Beighton Score Validity Article
Currently, there is no cure—but there are many treatment types that can improve symptoms. A proper diagnosis allows the patient and their doctor to communicate well and come up with a good treatment plan.
There are always studies ongoing about EDS and related disorders. BJCSF hosted the 2025 Together We Thrive Summit in Washington, DC that included many presentations about this research. Check out the Thrive recap and watch full presentations.
