Alternating Hemiplegia of Childhood: The Genetic Epilepsy That Doesn’t Yet Make Sense - Alexis Arzimanoglou & Rosaria Vavassori, EpiCARE & IAHCRC

For the 10-year anniversary of its gene mutation identification, learn about the ultra-rare epilepsy: Alternative Hemiplegia of Childhood. Rosaria Vavassoria and Prof. Alexis Arzimanoglou talk about their work to improve the lives of the families affected and indeed how far the understanding of AHC has come over the past decade.

  • Alexis is a paediatric and epileptological neurologist consultant, lead of the European Reference Network for EpiCARE, coordinator of the Epilepsy Program of the Epilepsy Unit at SJD Barcelona Children's Hospital, director of the Epilepsy, Sleep and Pediatric Neurophysiology Department at the University Hospitals of Lyon, France; and so many other things!

    Rosaria is the founder of AHC Europe, mum to a son with AHC, part of the EpiCARE European Patient Advocacy Group, data manager at the IAHCRC International Consortium; and so many other things!

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