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|Title:||Rates of Status Epilepticus and Sudden Unexplained Death in Epilepsy in People With Genetic Developmental and Epileptic Encephalopathies.||Austin Authors:||Donnan, Alice M;Schneider, Amy L ;Russ-Hall, Sophie;Churilov, Leonid ;Scheffer, Ingrid E||Affiliation:||Epilepsy Research Centre
Medicine (University of Melbourne)
The Florey Institute of Neuroscience and Mental Health
Melbourne Medical School, Faculty of Medicine, Dentistry and Health Sciences, The University of Melbourne, Parkville, Australia.
|Issue Date:||7-Feb-2023||Date:||2023||Publication information:||Neurology 2023; 100(16)||Abstract:||The genetic developmental and epileptic encephalopathies (DEEs) comprise a large group of severe epilepsy syndromes, with a wide phenotypic spectrum. Currently, the rates of convulsive status epilepticus (CSE), non-convulsive status epilepticus (NCSE) and sudden unexplained death in epilepsy (SUDEP) in these diseases are not well understood. We aimed to describe the proportions of patients with frequently observed genetic DEEs who developed CSE, NCSE, mortality and SUDEP. Understanding the risks of these serious presentations in each genetic DEE will enable earlier diagnosis and appropriate management.||URI:||https://ahro.austin.org.au/austinjspui/handle/1/32146||DOI:||10.1212/WNL.0000000000207080||ORCID:||0000-0003-1745-7982
|Journal:||Neurology||PubMed URL:||36750385||ISSN:||1526-632X||Type:||Journal Article|
|Appears in Collections:||Journal articles|
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checked on Dec 3, 2023
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