Want to learn more?
A new diagnosis can be so overwhelming. Because ZMYND11 is so rare, there is not a lot information out there for individuals and families. We are working to linking all research articles here in one place.
Most Recent Family Education Conference
If you were not able to make the most recent education conference, we have linked the videos below to catch up.
Genetics Overview by Nicolas Abreu, MD
Speech Disorders by Kristina Johnson, PhD
Finding a Treatment by Ethan Perlstein, PhD
Registry and Foundation Updated by Disa Vice
Autism by Taylor Day, PhD
Seizures by Amelle Shillington, DO
Introduction by Disa Vice
We encourage all those with ZMYND11 to join our patient registry with Combined Brain here.
Our goal is to find treatments that improve the function of the ZMYND11 protein, to decrease the severity of symptoms caused by the disorder.
When you have a rare disease, you face two battles: one, the illness itself, and the other, living in a world world where so few people know what you are up against— #raredisease
