Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/26103
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dc.contributor.authorBalestrini, Simona-
dc.contributor.authorArzimanoglou, Alexis-
dc.contributor.authorBlümcke, Ingmar-
dc.contributor.authorScheffer, Ingrid E-
dc.contributor.authorWiebe, Samuel-
dc.contributor.authorZelano, Johan-
dc.contributor.authorWalker, Matthew C-
dc.date2021-02-01-
dc.date.accessioned2021-03-24T21:39:05Z-
dc.date.available2021-03-24T21:39:05Z-
dc.date.issued2021-02-01-
dc.identifier.citationEpileptic Disorders 2021; 23(1): 1-16en
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/26103-
dc.description.abstractThe identification of the aetiology of a patient's epilepsy is instrumental in the diagnosis, prognostic counselling and management of the epilepsies. Indeed, the aetiology can be important for determining the recurrence risk of single seizures and so for making a diagnosis of epilepsy. Here, we divide the aetiologies into six categories: structural, genetic, infectious, metabolic, immune (all of which are part of the International League Against Epilepsy [ILAE] classification system) and neurodegenerative (which we have considered separately because of its growing importance in epilepsy). These are not mutually exclusive categories and many aetiologies fall into more than one category. Indeed, genetic factors probably play a role, to varying degrees, in the risk of seizures in all people with epilepsy. In each of the categories, we discuss what we regard as the most important aetiologies; importance being determined not only by prevalence but also by clinical significance. The introduction contains information suitable for level 1 competency (entry level), whilst the subsequent sections contain information aimed at level 2 competency (proficiency level) as part of the new ILAE competency-based curriculum. As we move towards precision medicine and targeted therapies, so aetiologies will play an even greater role in the management of epilepsy.en
dc.language.isoeng-
dc.subjectgeneticen
dc.subjectimmuneen
dc.subjectinfectiousen
dc.subjectmetabolicen
dc.subjectneurodegenerativeen
dc.subjectstructuralen
dc.titleThe aetiologies of epilepsy.en
dc.typeJournal Articleen
dc.identifier.journaltitleEpileptic Disordersen
dc.identifier.affiliationUCL Queen Square Institute of Neurology, Member of the ERN EpiCARE, London, UK, Chalfont Centre for Epilepsy, Bucks, UKen
dc.identifier.affiliationCumming School of Medicine, University of Calgary, Canadaen
dc.identifier.affiliationDepartment of Paediatric Clinical Epileptology and Functional Neurology, University Hospitals of Lyon (HCL), Member of the ERN EpiCARE, Lyon, France, Epilepsy Research Program, Epilepsy Unit, San Juan de Dios Paediatric Hospital, Member of the ERN EpiCARE, Barcelona, Spainen
dc.identifier.affiliationUniversity of Melbourne and Royal Children's Hospital, Florey and Murdoch Children's Research Institutes, Melbourne, Australiaen
dc.identifier.affiliationInstitute of Neuropathology, University Hospitals Erlangen, Collaborating Partner of the ERN EpiCARE, Erlangen, Germanyen
dc.identifier.affiliationSahlgrenska Academy and University Hospital, Member of the ERN EpiCARE, Gothenburg, Sweden, Wallenberg Center for Molecular and Translational Medicine, Gotenburg, Swedenen
dc.identifier.affiliationUCL Queen Square Institute of Neurology, Member of the ERN EpiCARE, London, UKen
dc.identifier.affiliationAustin Healthen
dc.identifier.doi10.1684/epd.2021.1255en
dc.type.contentTexten
dc.identifier.pubmedid33720020-
local.name.researcherScheffer, Ingrid E
item.fulltextNo Fulltext-
item.openairetypeJournal Article-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.grantfulltextnone-
item.languageiso639-1en-
item.cerifentitytypePublications-
crisitem.author.deptEpilepsy Research Centre-
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