Charity Overview
The Cute Syndrome Foundation (TCSF) raises awareness of rare SCN8A genetic mutations, works to advance SCN8A research, and supports individuals and families affected by SCN8A-related disorders. SCN8A mutations cause a range of neurological conditions, including epilepsy, developmental delay, movement disorders, autism spectrum disorder, and other physical and behavioural challenges. TCSF serves families affected by SCN8A in 56 countries around the world, empowering them with education, resources, and community.