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

The syndrome caused by germinal mutations in the WWOX gene is a neurological disorder associated with refractory epilepsy, seizure disorder associated with global developmental delay, progressive microcephaly, bilateral optic atrophy, and spastic quadriplegia.

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

Rami Aqeilan, PhD, Hebrew University of Jerusalem, Jerusalem, Israël, ramiaq@mail.huji.ac.il