Identification of a novel variant p.Ser606Gly in SCN3A associated with childhood absence epilepsy.

Wei Li, Wenli Zhao, Jing Wang, Xiaoli Zhang, Xinlai Qian, Renjun Gu, Guoyang He

Epilepsy research 2021 Sep

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Sodium (Na+) channels are the basis for action potential generation and propagation, which play a key role in the regulation of neuronal excitability. SCN3A is a gene encoding for sodium channel protein type 3 subunit alpha (or known as Nav1.3). This study aimed to explore SCN3A genetic variants in a cohort of childhood absence epilepsy (CAE) via whole exome sequencing. A novel SCN3A missense variant (c.A1816G, p.Ser606Gly) was identified in a patient with CAE. This variant had not been reported in both 1000G and ExAC databases. Bioinformatics analysis revealed that this variant was pathogenic and could transform the protein structure of Nav1.3. The reported phenotypes of SCN3A-related central nerve system disorders included multiple seizure types, polymicrogyria and different degrees of developmental delay/intellectual disability. The patient with p.Ser606Gly variant exhibited typical absence seizures. The MRI and CT scan results were normal, and EEG showed that 3-Hz spike-slow wave discharges. In conclusion, our findings not only broaden the pathogenic spectrum of SCN3A, but also extend the clinical phenotypes of SCN3A-related CAE. Copyright © 2021 Elsevier B.V. All rights reserved.

Citation

Wei Li, Wenli Zhao, Jing Wang, Xiaoli Zhang, Xinlai Qian, Renjun Gu, Guoyang He. Identification of a novel variant p.Ser606Gly in SCN3A associated with childhood absence epilepsy. Epilepsy research. 2021 Sep;175:106682