Ehlers-Danlos Syndrome Report

Ehlers-Danlos SyndromeEhlers-Danlos syndrome (EDS) is a group of inherited connective tissue disorders that affect the skin, joints, and blood vessels. EDS can cause hypermobility, joint pain, and other symptoms. This report tests for genetic variants that are known to affect collagen production and maintenance, as well as genes involved in other connective tissue components.More than 45 genes analyzed It is recommended if: This report is designed for individuals with a family history of EDS or individuals with symptoms of the condition. Genetic testing can confirm a diagnosis, provide information on disease severity and progression, and inform treatment and management decisions. Testing can also inform family planning decisions and provide reassurance for unaffected family members. List of main conditions: Ehlers-Danlos Syndrome