Introduction
Explore the videos below from a webinar entitled “Differential diagnosis and search for etiology in epilepsy and paroxysmal movement disorders”, where you will get the opportunity to learn more about navigating within the diagnostic journey for patients with epilepsy and an unknown etiology, different options of genetic investigations, clinical examples of finding the correct diagnosis and what this can mean to the patients and families.
M.D. PhD., Senior consultant in Child Neurology and Head of the Pediatric Epilepsy Team at Karolinska University Hospital / Astrid Lindgrens Children´s Hospital, Sweden
Differential diagnosis and search for etiology in epilepsy and paroxysmal movement disorders – Phenotyping is essential … but not enough
SE-AADC-0293
Neurologist, Associate Professor, Lead of Epilepsy Genetics Research Group at VIB Centre of Molecular
Neurology, University of Antwerp, Belgium
Genetic diagnosis in individuals with epilepsy and paroxysmal movement disorders – Importance of re-evaluating genetic testing results
SE-AADC-0294
SE-AADC-0295 | January 2023