OUR MISSION
The SATB2 Gene Foundation, Inc. was established to enrich the lives of individuals with SATB2-associated syndrome, including those diagnosed with the condition and their families, through support, research and education. Our mission will be met by raising awareness about the characteristics of SATB2-associated syndrome, providing support to families, and supporting research in a wide range of issues related to SATB2-associated syndrome.
SATB2 NEWS & ARTICLES
SAS Speech and Language Survey Report
SAS Speech & Language Survey Report In order to support families with a SAS diagnosis, in June 2021 an independent study supported by the SATB2 Gene Foundation was launched to better understand
Interview Study: Behaviours
Interview Study: Behaviours that Challenge in SATB2-associated syndrome Researchers at Aston University are conducting an interview study that aims to find out more about behaviours that challenge in SATB2-associated syndrome. We would
DRUG REPURPOSING SURVEY
DRUG REPURPOSING ROADMAP SURVEY Dear SATB2-Associated Syndrome Community, We would appreciate your insight on a new project! The SATB2 Gene Foundation is participating in partnership with the Castleman Disease Collaborative Network (CDCN)
SAS Family Assistance Program
SATB2 GENE FOUNDAION FAMILY ASSISTANCE PROGRAM Let’s face it. Providing for your SAS loved one can get expensive. If you need assistance, the SATB2 Gene Foundation may be able to help. We