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.

KAT6A and KAT6B syndromes are recognized globally. However, due to limited research and understanding, the true prevalence might be underestimated. These rare genetic conditions affect gene regulation during development, leading to diverse developmental, speech, feeding, and medical challenges. The KAT6 Foundation is committed to advancing care, research, and support for this growing community.