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Article

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

6 Nov 2020

Abstract excerpt

Objective To analyze the electroclinical characteristics, 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 mechanism of EAS. Methods A retrospective study was conducted on the participants diagnosed with Landau-Kleffner syndrome (LKS),...

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PMID: 33240831
DOI: 10.3389/fped.2020.574803

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