NeONATAL epilepsies / EESB

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call for collaborations

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Neonatal epilepsies with suppression burst pattern are rare, especially the forms with normal MRI and normal metabolic screening. This is the reason why we are looking for additional cases to increase the size of our cohort and to go faster in the identification of genetic causes for these diseases. As of january 2018, we have collected biological samples for 658 cases and found a genetic cause in 185 cases (28%).



To participate, we invite you to contact
Dr Mathieu Milh , who is coordinating the project.



Please contact us before sending any biological material since we are following very strict rules to comply with the french regulations.