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TBRS Community is Awarded NORD COVID-19 Rapid Response Seed Grant

We are excited to announce that The Tatton Brown Rahman Syndrome Community has been awarded the NORD COVID-19 Rapid Response Seed Grant. The funding will be...


Seeking Nominations for Katherine McMahon Memorial Award

Katherine McMahon was a founding board member of The Tatton Brown Rahman Syndrome Community. She followed the stories of each person affected by TBRS like...


New study looks at DNMT3A mosaicism

Dr. Ayala Tovy, a researcher at Baylor College of Medicine and a medical advisory board member of The TBRS Community, and her colleagues have described an...


New tool assesses COVID-19 risk for adults with rare diseases

The British Society for Genetic Medicine and the Clinical Genetics Society have developed an online tool to help determine the risks of COVID-19 for adults...


UK study on COVID-19 seeks rare disease participants

The CoIN study is looking into how the coronavirus pandemic is affecting the lives of children with rare diseases living in the UK. The researchers are seeking...


Research opportunity to share pandemic’s effects

The Rare Diseases Clinical Research Network, which is funded by the US National Institutes of Health, is gathering information from individuals with rare...


The Tatton Brown Rahman Syndrome Community joins NORD

The National Organization for Rare Disorders (NORD) has welcomed The TBRS Community as a member, joining 300 other patient organizations. NORD is a leading...


New study on function of DNMT3A variant

Researchers at the University of California, Riverside, have examined the function of a particular mutation in the DNMT3A gene called R882H. This variant is a...


Research opportunity from the Simons Foundation

Simons Searchlight is looking for individuals with variants in the DNMT3A gene, which causes Tatton Brown Rahman Syndrome, to participate in its study on the...