Overcoming the most pressing diagnostic challenges in epilepsy
Epilepsy has a profound effect on patients, families and carers. Furthermore, the burden to healthcare providers is enormous, with a number of unmet clinical needs impacting outcomes for patients. As a result, the field is now utilizing genomic data to investigate the genetic causes of epilepsy and many other rare disorders.
This guide provides you with a quick introduction to the most pressing unmet needs in epilepsy and how the use of genomic medicine is helping to overcome them.