This website provides information on patients with mutations in the KCNC2 gene, including clinical data, molecular data, management and research options.

The syndrome caused by mutations in the KCNC2 gene is a multisystem disorder characterized by a broad spectrum of more benign (genetic generalized epilepsy) to severe epilepsy like developmental and epileptic encephalopathy (DEE) including intractable seizues and disturbance of psycho-motor development.
Not all individuals with a mutation in the KCNC2 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 KCNC2 gene.

Yvonne Weber, MD, Dpt. of Epileptology and Neurology, University Clinic RWTH Aachen, Aachen, Germany, yweber@ukaachen.de

Stefan Wolking, MD, Dpt. of Epileptology and Neurology, University Clinic RWTH Aachen, Aachen, Germany