Who are we?
The FamilieSCN2A Foundation was founded in 2015 by parents of children diagnosed with rare forms of epilepsy and autism as a result of a change in the SCN2A gene. The SCN2A gene helps regulate neuronal excitability, support brain development, and contribute to learning and memory. Changes in the SCN2A gene can cause a range of health issues known as SCN2A-related disorders (SRD). LEARN MORE.
