Thank you for expressing interest in joining the KAT6 Foundation community. The KAT6 Foundation supports families and individuals diagnosed with KAT6 syndrome (caused by KAT6A and KAT6B variants) and advances research to develop treatments for KAT6 syndrome.
In order to help share important research information, community events, and support services we ask you to fill out the brief survey below.
We will not share this information with anyone outside our community. Having this basic information is vital to advancing our mission.
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The KAT6 Foundation was founded in 2017. We are a small, organization that is entirely led by fellow KAT6 parents who volunteer their time. We hope you will join us in supporting our children and families.