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.
What is SATB2-Associated Syndrome?
SATB2-associated syndrome (aka Glass Syndrome) is caused by problems in the SATB2 gene located on chromosome 2q33.1, which is a neurodevelopmental disorder. SAS affects the individuals through global developmental delays. Most significant is the absence of speech, or significantly delayed/affected speech. We often see palate abnormalities – including cleft palate or high arched palate. Other key characteristics of SAS are dental issues – missing adult teeth and/or oversized front teeth; low bone density, and behavioral issues. We are seeing a growing number of our patients with seizures and sleep difficulties.
SATB2 NEWS & ARTICLES
A New Chapter: Hiring our First Executive Director
The SATB2 Gene Foundation is excited to share an important milestone: we are hiring our first Executive Director. Since our founding, the Foundation has been led by dedicated volunteers, families, and advocates working together to
2026 SATB2 Conference Registration is OPEN
The SATB2 Gene Foundation Family & Medical Conference will take place July 22–24, 2026, in Oklahoma City, Oklahoma, presented by Dignity Memorial. Don’t miss the opportunity to join families, researchers, clinicians, and advocates from across the country and
Be a Partner in Impact – Sponsor the 2026 SATB2 Family Conference
We are thrilled to announce that the 2026 SATB2 Gene Foundation Family & Medical Conference will take place July 22–24, 2026, in Oklahoma City, Oklahoma! This biennial event brings together families, researchers, clinicians, and advocates
What is SATB2-Associated Syndrome Video
As we gear up to celebrate Rare Disease Day on February 28, we’re coming together all month long to honor the strength, resilience, and unity of the rare disease community.To kick off our Rare Disease