“What is the cause of my epilepsy?”

The role of genomics has been well established in epilepsy, initially with family and twin studies and then with the discovery of single genes causing epilepsy. What has evolved is that the vast majority of epilepsy patients have a more complex genomic basis for their epilepsy.

By integrating genomic testing into clinical care, we can provide a better understanding of the cause of epilepsy for a particular patient. This approach will end the diagnostic odyssey of searching for how and why they developed epilepsy and will enable precision-based, personalised treatment approaches based on the individual’s genomic results.