This website provides information on patients with mutations in the CYFIP2 gene, including clinical data, molecular data, management and research options.

The syndrome caused by mutations in the CYFIP2 gene is a multisystem disorder characterized by developmental delay / intellectual disability, seizures and abnormal muscle tone.
Not all individuals with a mutation in the CYFIP2 gene have these features.

This website was created to share and collect information about clinical, management and research projects to gather more knowledge and provide better treatment of patients with mutations in the CYFIP2 gene

Anais Begemann, MD, PhD, University of Zurich, Institute of Medical Genetics, Schlieren-Zurich, Switzerland, anais.begemann@medgen.uzh.ch

Anita Rauch, MD, University of Zurich, Institute of Medical Genetics, Schlieren-Zurich, Switzerland, anita.rauch@medgen.uzh.ch