SKS
SKS
Improving the lives of all people impacted by Smith-Kingsmore syndrome
Investing in groundbreaking research to accelerate understanding and treatment of Smith-Kingsmore Syndrome
The mission of the Smith-Kingsmore Syndrome Foundation is to improve the lives of all people impacted by Smith-Kingsmore syndrome by accelerating research and connecting our global community. Our vision is a world cured of Smith-Kingsmore syndrome. Working together we can change outcomes.
Smith-Kingsmore syndrome (SKS) is a mutation of the mTOR gene that stops the brain from developing and functioning properly, leading to intellectual, developmental, behavioral and physical issues. The most common features of SKS are intellectual and developmental disability, large brain size, sleep disturbances, seizures and autism.
Learn More
You are not alone. The Smith-Kingsmore Syndrome Foundation and our broader community are here to support you.
Family Guide >>
The Smith-Kingsmore Syndrome Foundation is the only global non-profit organization investing in research to find treatments and a cure for SKS.
LEARN MORE >>
Joining our patient registry is an important way to contribute to our knowledge of Smith-Kingsmore syndrome, and gather the data we need to drive research forward.
LEARN MORE >>Donating to the Smith-Kingsmore Syndrome Foundation is a powerful act of hope. Your donation drives investment in cutting-edge research and efforts to collaborate and build community across the world. Together we can improve the lives of everyone impacted by Smith-Kingsmore syndrome.
DonateFamilies
Connected In
43 Countries
Invested In
SKS Research
NIH grant
to our research
network
Research
& Family
Conferences
Hosted
SKS Guides
Published
In 23
Languages
