Current SCN2A Research

Would you like your child or family member with SCN2A related epilepsy to participate in research studies? A study might include an online survey or phone interview, past medical records, EEG and MRI reports, lab reports, or possible blood tests and other medical procedures.

The FamilieSCN2A Foundation believes research is our best hope new treatments and eventually finding a cure for SCN2A associated epilepsies. Your family member or child’s participation can help us work toward these goals.

If you are interested in participating in research to help find treatment and a cure for SCN2A, please review the current research projects we have in place. These projects help get us closer to understanding this complex sodium channel disorder and closer to improving treatment and finding a cure. Participation is completely voluntary for anyone who has been diagnosed with an SCN2A gene mutation, deletion, or replication.