KAT6 Known Cases

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Join the KAT6A/KAT6B patient registry

to support research, stay informed, identify cases and find a treatment

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Make a Difference

Help us support people and their families living with KAT6A and KAT6B syndromes. Your donations will fund vital research into KAT6A and KAT6B gene mutations and provide assistive equipment and therapies to families through our Empowered grants. All donations are tax deductible in the US and go to KAT6 Foundation, a nonprofit 501(c)(3).


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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.

#Driving Research

The KAT6 Foundation proudly funds and supports international research by connecting families to current research studies.

#Assisting Families

An Empowered Grant provides funding for the purchase of assistive equipment and therapy treatment to individuals diagnosed with KAT6A and KAT6B syndromes.

#raising Awareness

We strive to support individuals diagnosed with KAT6 syndromes by raising awareness and advocating for acceptance and inclusion worldwide.

Rare Disease Day 2026: February 28th

It’s time to gear up for International Rare Disease Day! We invite you to wear stripes and KAT6 awareness clothing to show your solidarity with our ultra-rare community. Last year, families across the KAT6 community advocated for Rare Disease Day in their local communities, schools, and even in the press. We hope you will join […]

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