This website provides information on patients with mutations in the CCND2 gene, including clinical data, molecular data, management and research options.

Disorders caused by mutations in the CCND2 gene include the following:

• The megalencephaly-polymicrogyria-polydactyly-hydrocephalus (MPPH) syndrome.

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 CCND2 gene.

Ghayda Mirzaa, MD, University of Washington School of Medicine, Seattle, Washington, USA, Ghayda.mirzaa@seattlechildrens.org

William B. Dobyns, MD, University of Washington School of Medicine, Seattle, Washington, USA, wbd@uw.edu