top of page
.jpeg)
What is Rubinstein-Taybi Syndrome?
Rubinstein-Taybi Syndrome is a rare genetic syndrome that affects 1 in every 125,000 children. It is a mutation of the CREBBP (Type 1) or EP300 (Type 2) gene. Children and adults with RTS have developmental and cognitive delays. Below are some resources to learn more about RTS.
.jpeg)
**We are not medical professionals. All information provided on this site is from RTS resources. We encourage those with questions to consult a medical professional.
bottom of page