WEST Syndrome Report

WEST SyndromeWEST syndrome is a rare epilepsy syndrome that typically affects infants. WEST syndrome is caused by mutations in genes involved in the development and function of the brain, and this report tests for genetic variants that are known to affect these processes.1 gene analyzed genes analyzed It is recommended if: This report is designed for individuals with a family history of WEST syndrome or individuals with symptoms of the condition, such as infantile spasms, developmental delay, and cognitive impairment. 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: WEST Syndrome