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WELCOME
FamilieSCN2A is an organization created by parents of children diagnosed with
rare forms of Epilepsy and Autism as a result of a change in the SCN2A gene.
Our goal is to find a cure!
*Photo courtesy Ra Design & Photography
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Seizure Disorders Associated with SCN2A
Epilepsy, Benign Familial Infantile Seizures (type 3), Early Infantile Epileptic Encephalopathy (type 11), Otahara, West Syndrome, Generalized Epilepsy with Febrile Seizures, Migrating Partial Epilepsy of Infancy (MPEI)
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