Development of criteria for epilepsy genetic testing in Ontario, Canada

Puneet Jain, Danielle Andrade, Elizabeth Donner, David Dyment, Asuri N. Prasad, Sharan Goobie, Kym Boycott, Matthew Lines, O. Carter Snead

Résultat de recherche: Review articleexamen par les pairs

20 Citations (Scopus)

Résumé

Multiple genes/variants have been implicated in various epileptic conditions. However, there is little general guidance available on the circumstances in which genetic testing is indicated and test selection in order to guide optimal test appropriateness and benefit. This is an account of the development of guidelines for genetic testing in epilepsy, which have been developed in Ontario, Canada. The Genetic Testing Advisory Committee was established in Ontario to review the clinical utility and validity of genetic tests and the provision of genetic testing in Ontario. As part of their mandate, the committee also developed recommendations and guidelines for genetic testing in epilepsy. The recommendations include mandatory prerequisites for an epileptology/geneticist/clinical biochemical geneticist consultation, prerequisite diagnostic procedures, circumstances in which genetic testing is indicated and not indicated and guidance for selection of genetic tests, including their general limitations and considerations. These guidelines represent a step toward the development of evidence-based gene panels for epilepsy in Ontario, the repatriation of genetic testing for epilepsy into Ontario molecular genetic laboratories and public funding of genetic tests for epilepsy in Ontario.

Langue d'origineEnglish
Pages (de-à)7-13
Nombre de pages7
JournalCanadian Journal of Neurological Sciences
Volume46
Numéro de publication1
DOI
Statut de publicationPublished - janv. 1 2019
Publié à l'externeOui

Note bibliographique

Publisher Copyright:
Copyright © The Canadian Journal of Neurological Sciences Inc. 2018.

ASJC Scopus Subject Areas

  • Neurology
  • Clinical Neurology

PubMed: MeSH publication types

  • Journal Article
  • Review

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