Clinical Forms and GRIN2A Genotype of Severe End of Epileptic-Aphasia Spectrum Disorder

Clinical Forms and GRIN2A Genotype of Severe End of Epileptic-Aphasia Spectrum Disorder

Objective: This study aims to analyze the electroclinical characteristics and gene test results of children on the severe end of the epilepsy aphasia spectrum (EAS) and also the correlation of EAS-related GRIN2A genes to explore the genotype-phenotype relationships, as well as potential pathogenic m...

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Bibliographic Details
Main Authors: Xiao Li, Ling-Ling Xie, Wei Han, Si-Qi Hong, Jian-Nan Ma, Juan Wang, Li Jiang
Format: Article
Language:English
Published: Frontiers Media S.A. 2020-11-01
Series:Frontiers in Pediatrics
Subjects:
Landau-Kleffner syndrome (LKS)
epileptic encephalopathy with continuous spike-and-wave during sleep (CSWS)
atypical benign partial epilepsy (ABPE)
genotype-phenotype relationship
epileptic-aphasia spectrum disorder
Online Access:https://www.frontiersin.org/articles/10.3389/fped.2020.574803/full

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https://www.frontiersin.org/articles/10.3389/fped.2020.574803/full

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