ILAE Genetic Literacy Series: familial focal epilepsy syndromes.


Journal

Epileptic disorders : international epilepsy journal with videotape
ISSN: 1950-6945
Titre abrégé: Epileptic Disord
Pays: United States
ID NLM: 100891853

Informations de publication

Date de publication:
01 Apr 2022
Historique:
pubmed: 11 12 2021
medline: 25 5 2022
entrez: 10 12 2021
Statut: ppublish

Résumé

There are a number of familial focal epilepsy syndromes, each with distinct clinical characteristics. Here, we review the epilepsy phenotypes and the genetic architecture of these syndromes. Using an illustrative clinical case, we describe the important steps in making a diagnosis and ordering appropriate genetic tests. Our discussion on the genetics of the familial focal epilepsies will provide a framework for interpreting the results of genetic testing, and allow us to apply this information to patient management.

Identifiants

pubmed: 34887240
pii: epd.2021.1393
doi: 10.1684/epd.2021.1393
doi:

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

221-228

Auteurs

Samuel Gooley (S)

Epilepsy Research Centre, Department of Medicine, University of Melbourne, Austin Health, Heidelberg, Victoria 3084, Australia, Department of Neurology, Northern Health, Epping, Victoria 3076, Australia.

Douglas E Crompton (DE)

Epilepsy Research Centre, Department of Medicine, University of Melbourne, Austin Health, Heidelberg, Victoria 3084, Australia, Department of Neurology, Northern Health, Epping, Victoria 3076, Australia.

Samuel F Berkovic (SF)

Epilepsy Research Centre, Department of Medicine, University of Melbourne, Austin Health, Heidelberg, Victoria 3084, Australia.

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Classifications MeSH