Registry Launched!
We are pleased to announce the launch of The Cute Syndrome Foundation Global SCN8A Survey Series! The Cute Syndrome Foundation Global SCN8A Survey Series creates a platform for patients around the world to strengthen their voices and share information about SCN8A disorders. SCN8A disorders currently has no cure. Designed with the input of scientists and patients, this global resource will provide data for researchers to use to advance drug development and treatment options to help improve SCN8A patient care.
Join now and let your data tell your story!
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