This website provides information on patients with mutations in the ZNF711 gene, including clinical data, molecular data, management and research options.

The syndrome caused by mutations in the ZNF711 gene is a multisystem disorder characterized by mild to moderate ID and poor speech accompanied by additional features in some patients, including autistic features and mild facial dysmorphisms.

Not all individuals with a mutation in the ZNF711 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 ZNF711 gene.

Frank Kooy, PhD, Department of Medical Genetics, University of Antwerp, Antwerp, Belgium, Frank.Kooy@uantwerpen.be

Anke Van Dijck, MD, Department of Medical Genetics, University of Antwerp, Antwerp, Belgium, Anke.VanDijck@uantwerpen.be