This website provides information on patients with mutations in the ADAT3 gene, including clinical data, molecular data, management and research options.

Mutations in the ADAT3 gene cause an autosomal recessive type of mental retardation that is usually associated with other abnormalities, such as strabismus, microcephaly, and poor growth. This website was created to share and collect information about clinic, management and research projects to deliver more knowledge and provide better treatment to patients with mutations in the ADAT3 gene.

Fowzan S. Alkuraya, MD (Hons) ABP ABMG (Clinical Genetics and Clinical Molecular Genetics), Department of Genetics, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia / Department of Anatomy and Cell Biology, College of Medicine, Alfaisal University, Riyadh, Saudi Arabia, falkuraya@kfshrc.edu.sa

Fadie D. Altuame, MBBS Candidate, College of Medicine, Alfaisal University, Riyadh, Saudi Arabia, faltuame@alfaisal.edu