FamilieSCN2A is an organization created by parents of children diagnosed with epilepsy and autism as a result of a change in the SCN2a gene. Our goal is to find a cure!
SCN2A is a sodium ion channel gene located on chromosome 2. Sodium ion channels are proteins in cells that allow sodium to pass to the inside. Sodium ion channels play a key role in a cell's ability to generate and transmit electrical signals.
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)
Seizure Disorders Associated with SCN2A
Autism Spectrum Disorder, Attention Deficit Hyperactivity Disorder, Global/Developmental Delays, Intellectual Disabilities, Schizophrenia, Movement and Speech Disorders, Dysautonomia, Dystonia, Gastrointestinal Issues, and Cortical Visual Impairment
Other Medical Challenges Associated with SCN2A
FamilieSCN2A Foundation Video
These are just some of the faces of children affected by a change in their SCN2A gene. The purpose of this video is to spread awareness to help further understand SCN2A and ultimately find a CURE!