KAT6 Foundation

The KAT6 Foundation was founded in 2017 by a handful of parents of children identified with mutations on their KAT6A gene. At the time, there were less than 50 known KAT6A cases. In the span of 5 years, our numbers have expanded to over 370 known KAT6A cases worldwide. In 2020, the KAT6A Foundation began fostering connections with the KAT6B community and in 2022, we formally became the KAT6 Foundation, an organization devoted to understanding mutations in both KAT6A and KAT6B genes. Today, there are more than 500 known cases of KAT6 syndromes worldwide, and we expect our numbers to continue to grow.