We are excited to announce the launch of the TBRS and DNMT3A Patient Registry

• We are excited to announce the launch of the TBRS and DNMT3A Patient Registry 2.0! The TBRS and DNMT3A Patient Registry creates a platform for patients around the world to strengthen their voices and share information about Tatton Brown Rahman Syndrome (TBRS), Heyn Sproul Jackson Syndrome (HESJAS), and DNMT3A-related disorders. All of these disorders involve DNMT3A gene variants, so study of them together may assist in furthering our understanding of them, separately and as a whole! Join now and let your data tell your story at tbrsregistry.iamrare.org!
• Make a difference in our community! Take the time to complete the TBRS Community Patient Registry surveys so we can start to understand TBRS and work toward developing treatments. Go to tbrsregistry.iamrare.org.
• Our TBRS Summit really demonstrated the importance of the registry to researchers! Participate in research at tbrsregistry.iamrare.org.