Epilepsy Phenome/Genome Project (EPGP)
EPGP is a team of 13 clinical centers across the United States working in collaboration with the National Institutes of Health and various organizations devoted to the care of patients with epilepsy. The study will include 1500 pairs of siblings with generalized or localization-related epilepsy, 1500 controls who do not have epilepsy, and 750 patients with rare epilepsies along with their parents. Everyone who volunteers for EPGP will be asked to give a sample of their DNA via a blood draw, and answer some questions asked by a study nurse or physician.
You may be eligible to participate in this study if you:
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Are between the ages of 4 weeks and 60 years old
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Have been diagnosed with IGE or LRE and have a sibling with epilepsy
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Have been diagnosed with IS, LGS, PVH, or PMG and both of your parents can volunteer
You will be excluded from this study if you:
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have epilepsy as a result of head injuries, stroke, brain infection, other known causes of seizures or epilepsy
This is a partial list of eligibility requirements. To inquire about your eligibility, please call the contact number provided. If you wish to inquire via e-mail, please include the title of the study in your message.