We are pleased to announce the launch of the KAT6A/KAT6B Patient Registry!

We are pleased to announce the launch of the KAT6A/KAT6B Patient Registry! The KAT6A/KAT6B Patient Registry creates a platform for patients around the world to strengthen their voices and share information about KAT6A/KAT6B Syndrome. Symptoms in KAT6A Syndrome often include global developmental delay, intellectual disability, hypotonia, speech and language deficits, gastrointestinal problems (such as feeding difficulties and constipation), and heart abnormalities. KAT6B Syndrome (which includes Genitopatellar syndrome and Say-Barber-Biesecker-Young-Simpson syndrome) typically manifests with developmental delay, intellectual disability, hypotonia, and skeletal, genital, and craniofacial abnormalities. Both KAT6A and KAT6B Syndromes currently have no cure.

Designed with the input of scientists and patients, this global resource will provide data for researchers to advance drug development and treatment options and help improve patient care in both KAT6A and KAT6B Syndrome.

Join now and let your data tell your story!