Recent advances in epilepsy genomics and genetic testing
- PMID: 32201576
- PMCID: PMC7076331
- DOI: 10.12688/f1000research.21366.1
Recent advances in epilepsy genomics and genetic testing
Abstract
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.
Keywords: Chromosomal microarray; Developmental and epileptic encephalopathy; Epilepsy; Gene panels; Genetic testing; Next generation sequencing; Novel genes; Whole genome sequencing.
Copyright: © 2020 Hebbar M and Mefford HC.
Conflict of interest statement
No competing interests were disclosed.No competing interests were disclosed.No competing interests were disclosed.
Similar articles
-
Yield of exome sequencing in patients with developmental and epileptic encephalopathies and inconclusive targeted gene panel.Eur J Paediatr Neurol. 2024 Jan;48:17-29. doi: 10.1016/j.ejpn.2023.10.006. Epub 2023 Nov 13. Eur J Paediatr Neurol. 2024. PMID: 38008000
-
Impact of genetic testing in developmental and epileptic encephalopathy- parents' perspective.Epilepsy Behav. 2025 Feb;163:110174. doi: 10.1016/j.yebeh.2024.110174. Epub 2024 Dec 22. Epilepsy Behav. 2025. PMID: 39709846
-
Operational definition of developmental and epileptic encephalopathies to underpin the design of therapeutic trials.Epilepsia. 2025 Apr;66(4):1014-1023. doi: 10.1111/epi.18265. Epub 2025 Feb 27. Epilepsia. 2025. PMID: 40013914 Free PMC article. Review.
-
Genetic investigations of the epileptic encephalopathies: Recent advances.Prog Brain Res. 2016;226:35-60. doi: 10.1016/bs.pbr.2016.04.006. Epub 2016 May 31. Prog Brain Res. 2016. PMID: 27323938 Review.
-
From next-generation sequencing to targeted treatment of non-acquired epilepsies.Expert Rev Mol Diagn. 2019 Mar;19(3):217-228. doi: 10.1080/14737159.2019.1573144. Epub 2019 Feb 4. Expert Rev Mol Diagn. 2019. PMID: 30661434 Review.
Cited by
-
Genetic Diagnosis Spectrum and Multigenic Burden of Exome-Level Rare Variants in a Childhood Epilepsy Cohort.Front Genet. 2021 Dec 21;12:782419. doi: 10.3389/fgene.2021.782419. eCollection 2021. Front Genet. 2021. PMID: 34992632 Free PMC article.
-
PlexinA1 deficiency in BALB/cAJ mice leads to excessive self-grooming and reduced prepulse inhibition.IBRO Rep. 2020 Oct 22;9:276-289. doi: 10.1016/j.ibror.2020.10.004. eCollection 2020 Dec. IBRO Rep. 2020. PMID: 33163687 Free PMC article.
-
Case report: Novel variants cause developmental and epileptic encephalopathy in three unrelated families from Mali.Front Genet. 2024 Nov 18;15:1412442. doi: 10.3389/fgene.2024.1412442. eCollection 2024. Front Genet. 2024. PMID: 39624497 Free PMC article.
-
Genomic Investigation of Infantile and Childhood Epileptic Encephalopathies in Kazakhstan: An Urgent Priority.Front Neurol. 2021 Jun 10;12:639317. doi: 10.3389/fneur.2021.639317. eCollection 2021. Front Neurol. 2021. PMID: 34177756 Free PMC article.
-
Pharmacological chaperones restore proteostasis of epilepsy-associated GABAA receptor variants.bioRxiv [Preprint]. 2023 Apr 19:2023.04.18.537383. doi: 10.1101/2023.04.18.537383. bioRxiv. 2023. Update in: Pharmacol Res. 2024 Oct;208:107356. doi: 10.1016/j.phrs.2024.107356. PMID: 37131660 Free PMC article. Updated. Preprint.
References
Publication types
MeSH terms
LinkOut - more resources
Full Text Sources
Other Literature Sources
Medical