Latest / The KCNA2 & Rare Epilepsy’s Podcast
Could a Patient Registry Bring KCNA2 Treatments Closer? Insights from Dr. Jan Henji Driedger
What can a patient registry really do for a rare disease community... and why does every family’s participation matter?
In this episode of The KCNA2 & Rare Epilepsy Podcast, host Dr. Nancy Musarra welcomes back Dr. Jan Henji Driedger, a physician-scientist and child neurologist involved in rare genetic epilepsy research at Heidelberg University Hospital in Germany.
Together, they explore the purpose of the KCNA2 patient registry and why registries are so important for rare and ultra-rare diseases. Dr. Driedger explains how structured, long-term data can help researchers better understand the…
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