Smith-Kingsmore Syndrome Foundation

The Smith-Kingsmore Syndrome Foundation is a registered 501(c)(3) non-profit organization, created by parents of children diagnosed with Smith-Kingsmore Syndrome. It is the only global organization funding SKS research and providing education and support to the Smith-Kingsmore syndrome community.

Our vision is a world cured of Smith-Kingsmore syndrome.

Our mission is to improve the lives of all people impacted by Smith-Kingsmore syndrome by accelerating research and connecting our global community.