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Professor Andreas Brunklaus, Consultant Paediatric Neurologist and Chief Investigator, tells us about the data collected and what study participation involves.
SCN1A Horizons is anticipated to be a milestone in transforming understanding of SCN1A epilepsies, including Dravet Syndrome, one of the most complex and severe developmental and epileptic conditions. The nationwide study aims to define the seizure, neuro-developmental, and behavioural characteristics of SCN1A-related epilepsies in 400 children and adults over a period of three years, with the goal of improving and standardising care across the UK.
For more information about the SCN1A Horizons Natural History Study, including information about participating centres, please contact the study team on SCN1AHorizons@glasgow.ac.uk.