KCNQ2 e.V.
managed by Björn Stavermann
About us
KCNQ2 is a gene that is important for the function of nerve cells in the brain. Mutations in this gene can lead to a range of neurological disorders that mainly occur in newborns and can range from mild seizures to severe, developmental epileptic encephalopathies.
The KCNQ2 Association is a point of contact for affected families. We offer insight into life with KCNQ2, provide advice on a wide range of topics, and have built up a large network. We organize parent meetings with scientific lectures and collect donations to support affected families in the care and support of their sick children.
Contact
Karl-Marx-Straße 8
54290
Trier
Germany
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