DOCK7

This website provides information on patients with mutations in the DOCK7 gene, including clinical data, molecular data, management and research options.

Developmental and epileptic encephalopathy 23, associated with variations of the DOCK7 gene is a multisystem epilepsy characterized by early onset seizures, mostly resistant to antiseizure treatment, severe neurodevelopmental retardation/ intellectual disability, typical facial features and cortical blindness.

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 DOCK7 gene.

Dilşad TÜRKDOĞAN, MD, Prof., Director, Marmara University Medical Faculty, Department of Pediatric Neurology, Istanbul, Turkey, dturkdogan@marmara.edu.tr, dturkdogan@hotmail.com

Terms & Conditions

Read More

Search Gene sites

Read More

Publications & News

Read More