The only 501(c)(3) founded to support the international KAT6 community.
Where we turn rare into resilient.
Where hope becomes action.
From diagnosis to destiny—together, we write a brighter story.
Stand with us, and we'll stand with you, as we change the landscape for families living with KAT6A and KAT6B syndromes.
KAT6A and KAT6B syndromes are newly recognized as rare genetic conditions that affect how genes are regulated during development. Changes in these genes can lead to developmental, speech, feeding, and medical differences that vary by person. Although only 700 cases have been diagnosed, this is a growing global community. The KAT6 Foundation drives better care, research, and support.
Registering adds your family’s voice to a growing movement. By sharing basic health and development information, you help researchers see patterns, accelerate studies, and improve care guidelines—while the Foundation keeps you informed about resources, trials, and community support. Every registration strengthens the data, widens the circle, and brings us closer to answers for KAT6A/KAT6B.
Our Mission
The KAT6 Foundation supports people and their families who are living with KAT6A and KAT6B syndromes around the world. We advance scientific research aimed at developing treatments and spread awareness of KAT6 syndromes so they can be more easily identified, treated and studied.
