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
Contact Registry and Resource Portal Access
CONTACT REGISTRY AND RESOURCE PORTAL ACCESS Are you a parent or caregiver of an individual with SATB2-associated syndrome (SAS)? Enroll in our contact registry to stay informed of available research opportunities, medical
Webinar Series
WEBINAR SERIES Be sure to check out our webinar series for valuable information on important topics ranging from speech and communication, AAC, estate planning, potty training, managing behaviors, and more! This webinar
2020 Research Grant Awards
2020 RESEARCH GRANT AWARDS The SATB2 Gene Foundation Board of Directors is pleased to announce the awardees for our 2020-2021 Research Grant Program: Sarah Vergult of Ghent University for her research project
Continuity of Care RARE Patient Impact Grant Program
CONTINUITY OF CARE RARE PATIENT IMPACT GRANT PROGRAM Update: Applications for this program are now closed. We are pleased, that through the generosity of Global Genes, we were able to support 14