KCNQ2 Registry

Dear KCNQ2 families, we are proud of the valuable project with Prof. Dr. Syrbe and his team from the University Hospital in Heidelberg!

The KCNQ2 Registry is of great importance to develop a better understanding of disease pathways, catalog the genetic variations and identify potential therapeutic approaches. It promotes the exchange of information between researchers, clinicians and patients, leading to improved diagnosis and treatment. This is why it is so important that many affected families participate, so that we can better understand the impact of the genetic defect and our children.

Anyone worldwide can participate. The register is available in German and English. Many other languages are close to completion.

Follow the link and take a look at the website. You will find further explanations and helpful FAQs there. Do you have any further questions? Then please contact info@kcnq2.de.

We look forward to using the KCNQ2 registry to find better therapies and medicines for our children in the future and to simplify the medical exchange.

Your KCNQ2 e.V. team