Epilepsy Phenome/Genome Project - First And Largest Research Study Of Its Kind To Understand What Causes Epilepsy

Main Category: Epilepsy
Article Date: 27 Oct 2008 - 6:00 PDT

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The Epilepsy Phenome/Genome Project (EPGP) consists of a group of researchers, physicians, coordinators, family members, people with epilepsy, advocates, and friends working together unlock the mysteries of epilepsy.

EPGP is the first and largest research study of its kind to understand what causes epilepsy, why people respond differently to medications, and why some families have several people with seizures. The National Institutes of Health is partnering with leading epilepsy professionals, advocacy groups, and families across the U.S. for this 5 year study.

The goal of EPGP is to collect, anonymously, a blood sample and detailed clinical information on people with specific types of epilepsy, in order to improve the diagnosis and treatment of epilepsy for many people living with seizures.

The study is looking for participants who:

1) Have epilepsy and also have a brother or sister with epilepsy
or
2) Have seizures due to Lennox-Gastaut Syndrome, Infantile Spasms, Polymicrogyria, or Periventricular Heterotopia. (No sibling required, but both parents must also agree to participate.)

Even if you do not qualify to participate, you can help by telling other people in the epilepsy community about this important project. In particulalr, please keep an eye out for siblings with epilepsy and ask them to contact us.

This study has the potential to change to future of epilepsy care for everyone, so please join us in the cause!

Epilepsy Phenome/Genome Project