We use essential cookies to make our site work. With your consent, we may also use non-essential cookies to improve user experience, personalize content, customize advertisements, and analyze website traffic. For these reasons, we may share your site usage data with our social media, advertising, and analytics partners. By clicking ?Accept,? you agree to our website's cookie use as described in our Cookie Policy. You can change your cookie settings at any time by clicking ?Preferences.?
It looks like your browser is outdated. Please update to the latest version in order to get a better experience.
The Cute Syndrome Foundation raises awareness of SCN8A genetic mutations, funds the dedicated and talented scientists researching SCN8A, and supports individuals and families around the world who are affected by SCN8A-related disorders.