This website provides information on patients with mutations in the SATB2 gene, including clinical data, molecular data, management and research options.

The syndrome caused by mutations in the SATB2 gene is a multisystem disorder characterized by developmental delay with severe speech delay, hypotonia, palate and dental abnormalities, behavioral difficulties, seizures, and skeletal anomalies.

Not all individuals with a mutation in the SATB2 gene have these features.

This website was created to share and collect information about clinic, management and research projects to gather more knowledge and provide better treatment of patients with mutations in the SATB2 gene.

Yuri Zarate, MD, University of Arkansas for Medical Sciences, Little Rock, AR, USA, yazarate@uams.edu