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
2020 Year in Review
2020 Year in Review What a year! 2020 certainly brought change to all of us. What started off as a year looking forward to being together for our 3rd annual SATB2 Family
2021 Conference Announcement and Planning Survey
Dear SATB2 Community: We hope that the welcome to a new year brings all of us much-needed positive changes from the current pandemic situation. Unfortunately, these changes are occurring more slowly than we wished for,
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