The SATB2 Gene Foundation, Inc. aims to enrich the lives of those affected by SATB2 associated syndrome and their families through promoting awareness, offering support, and supporting research into a wide range of related issues.
The SATB2 Gene Foundation's Research Grant Program is focused on advancing understanding and treatments for SATB2-associated syndrome (SAS), a rare neurogenetic disorder. It prioritizes research that generates pilot data to support larger grant applications, and focuses on areas such as speech and language development, behavior, sleep, and global developmental delays, among others. The foundation supports projects seeking foundational knowledge as well as those aiming for immediate clinical applicability, including but not limited to, studies on SATB2 function, clinical phenotype variations, and therapeutic interventions.