Tatton Brown Rahman Syndrome Community and National Organization for Rare Disorders Launch Natural History Study of Tatton Brown Rahman Syndrome
September 23, 2021
September 23, 2021
STANFORDVILLE, New York, Sept. 23 (TNSRes) -- The National Organization for Rare Disorders issued the following news release on Sept. 21, 2021:
Tatton Brown Rahman Syndrome Community and the National Organization for Rare Disorders, Inc. today launched the largest-ever study to research Tatton Brown Rahman Syndrome, a mutation of DNMT3A, that causes overgrowth, autism, intellectual disabilities, orthopedic concerns, cardiac issues, and a variety of other health and developmental sym . . .
Tatton Brown Rahman Syndrome Community and the National Organization for Rare Disorders, Inc. today launched the largest-ever study to research Tatton Brown Rahman Syndrome, a mutation of DNMT3A, that causes overgrowth, autism, intellectual disabilities, orthopedic concerns, cardiac issues, and a variety of other health and developmental sym . . .