SATB2 Gene Foundation

The SATB2 Gene Foundation is dedicated to improving the lives of individuals and families affected by SATB2-Associated Syndrome (SAS). SAS is a neurodevelopmental disorder caused by problems in the SATB2 gene, located on chromosome 2q33.1, and primarily causes global developmental delays, absence of speech or significantly affected speech, dental issues, low bone density, and behavioral issues. The SATB2 Gene Foundation was established to support SAS individuals and families through raising awareness, family support, and research, and is a rapidly growing organization expanding its reach, resources, and impact each year.