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Recent advances in epilepsy genomics and genetic testing

Developmental and epileptic encephalopathies (DEEs) are a group of severe, early onset epilepsies characterized by refractory seizures, developmental delay or regression associated with ongoing epileptic activity, and generally poor prognosis. DEE is genetically and phenotypically heterogeneous, and...

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Detalles Bibliográficos
Autores principales: Hebbar, Malavika, Mefford, Heather C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: F1000 Research Limited 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7076331/
https://www.ncbi.nlm.nih.gov/pubmed/32201576
http://dx.doi.org/10.12688/f1000research.21366.1
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author Hebbar, Malavika
Mefford, Heather C.
author_facet Hebbar, Malavika
Mefford, Heather C.
author_sort Hebbar, Malavika
collection PubMed
description Developmental and epileptic encephalopathies (DEEs) are a group of severe, early onset epilepsies characterized by refractory seizures, developmental delay or regression associated with ongoing epileptic activity, and generally poor prognosis. DEE is genetically and phenotypically heterogeneous, and there is a plethora of genetic testing options to investigate the rapidly growing list of epilepsy genes. However, more than 50% of patients with DEE remain without a genetic diagnosis despite state-of-the-art genetic testing. In this review, we discuss the major advances in epilepsy genomics that have surfaced in recent years. The goal of this review is to reach a larger audience and build a better understanding of pathogenesis and genetic testing options in DEE.
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spelling pubmed-70763312020-03-20 Recent advances in epilepsy genomics and genetic testing Hebbar, Malavika Mefford, Heather C. F1000Res Review Developmental and epileptic encephalopathies (DEEs) are a group of severe, early onset epilepsies characterized by refractory seizures, developmental delay or regression associated with ongoing epileptic activity, and generally poor prognosis. DEE is genetically and phenotypically heterogeneous, and there is a plethora of genetic testing options to investigate the rapidly growing list of epilepsy genes. However, more than 50% of patients with DEE remain without a genetic diagnosis despite state-of-the-art genetic testing. In this review, we discuss the major advances in epilepsy genomics that have surfaced in recent years. The goal of this review is to reach a larger audience and build a better understanding of pathogenesis and genetic testing options in DEE. F1000 Research Limited 2020-03-12 /pmc/articles/PMC7076331/ /pubmed/32201576 http://dx.doi.org/10.12688/f1000research.21366.1 Text en Copyright: © 2020 Hebbar M and Mefford HC http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution Licence, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review
Hebbar, Malavika
Mefford, Heather C.
Recent advances in epilepsy genomics and genetic testing
title Recent advances in epilepsy genomics and genetic testing
title_full Recent advances in epilepsy genomics and genetic testing
title_fullStr Recent advances in epilepsy genomics and genetic testing
title_full_unstemmed Recent advances in epilepsy genomics and genetic testing
title_short Recent advances in epilepsy genomics and genetic testing
title_sort recent advances in epilepsy genomics and genetic testing
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7076331/
https://www.ncbi.nlm.nih.gov/pubmed/32201576
http://dx.doi.org/10.12688/f1000research.21366.1
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