Epilepsy Panel Test code: 03401 • Up to 320 genes
Epilepsy Panel
This panel analyzes genes associated with both syndromic and non-syndromic forms of epilepsy, a common neurological disorder characterized by recurrent, unprovoked seizures.
Epilepsy can have many different genetic causes, and individuals with similar seizure types or clinical presentations may have different underlying genetic conditions. Comprehensive genetic testing allows for the evaluation of multiple potential genetic causes based on a single clinical indication.
Genetic testing may provide valuable information by helping to:
- Confirm or clarify a clinical diagnosis
- Identify an underlying genetic cause of epilepsy
- Distinguish between different genetic forms of epilepsy
- Support individualized treatment and medical management
- Help inform disease prognosis and potential progression
- Guide appropriate monitoring and surveillance
- Support earlier recognition of associated symptoms or complications
- Inform family planning and genetic counseling
- Identify potentially affected family members who may benefit from genetic testing
- Support consideration for relevant clinical trials
Some genes included in this panel may also be associated with additional medical conditions unrelated to epilepsy. These conditions are not included among the disorders specifically evaluated by this test.
Genetic test results should be interpreted in conjunction with the individual's medical history, seizure characteristics, neurological evaluation, family history, and other clinical findings to support appropriate diagnosis and management.