Advancing research and empowering families
KAT6A/KAT6B Patient Registry
The KAT6A/KAT6B Patient Registry is a secure database that provides a way to collect information from patients with KAT6A and KAT6B syndromes. The registry will provide new insights into the disease and identify areas for additional study and allow patients to be involved in improving the future of KAT6A and KAT6B syndromes.
For Patients
Get Involved
Information collected during this study may be used to help provide opportunities for patients and researchers to collaborate in the patient community.
For Researchers
Drive Research
This is a unique rare disease patient registry. Are you interested in using our data to further your research?