KCNA2 EPILEPSY

KCNA2 Epilepsy Global Alliance provides information and support for those who are diagnosed with KCNA2 and their families. Since the creation of our parent support group via Facebook in 2017, over 75 families from around the world have joined. Though there is currently no cure for KCNA2 Epilepsy, there is a need for advocacy, research opportunities, and effective treatment interventions... KCNA2 Epilepsy Global Connection provides information and support for those who are diagnosed with KCNA2. The goal of our site is to network with medical and scientific experts, neurologists, therapists, educators, and biopharmaceutical companies to advance research and treatment that will improve the quality of life and the treatments available for KCNA2 patients.   ... As of 2020, there is no cure and no FDA approved treatment for KCNA2. Current literature available about KCNA2 is often qualitative, and focused on identifying characteristics of those individuals diagnosed with KCNA2. The KCNA2..

Also known as: KCNA2 Epilepsy, Inc

Primary location: Independence United States