Ehlers-Danlos syndrome (EDS)
Ehlers-Danlos syndrome (EDS) is a group of inherited conditions that affect connective tissue, which can lead to a range of symptoms.
Types of Ehlers-Danlos syndrome (EDS)
There are 13 recognised types of EDS.
Some of the better-known types include classical EDS, Hypermobile EDS (hEDS), Vascular EDS and Kyphoscoliotic EDS. Hypermobile EDS (hEDS) is the most common type and accounts for around 90% of EDS cases.
Signs and symptoms
Symptoms vary depending on the type of EDS and can be different for each person.
Common symptoms can include:
- Very flexible (hypermobile) joints
- Joint pain and frequent injuries
- Muscle pain
- Fatigue
- Fragile or stretchy skin
- Slow healing or unusual scarring
How is Ehlers-Danlos syndrome (EDS) managed?
Management focuses on reducing symptoms, preventing complications, and improving quality of life. Care usually involves a team of healthcare professionals working together, along with self-management strategies to help manage symptoms.
For more information about EDS, please visit: