Li Ling, Yuan Lamei, Zheng Wen, Yang Yan, Deng Xiong, Song Zhi, Deng Hao
Health Management Center, The Third Xiangya Hospital, Central South University, Changsha, China.
Center for Experimental Medicine, The Third Xiangya Hospital, Central South University, Changsha, China.
Front Neurol. 2023 Jul 27;14:1229569. doi: 10.3389/fneur.2023.1229569. eCollection 2023.
Genetic epilepsy with febrile seizures plus (GEFSP) is a familial epileptic syndrome that is genetically heterogeneous and inherited in an autosomal dominant form in most cases. To date, at least seven genes have been reported to associate with GEFSP. This study aimed to identify the disease-causing variant in a Chinese Tujia ethnic family with GEFSP by using whole exome sequencing, Sanger sequencing, and prediction. A heterozygous missense variant c.5725A>G (p.T1909A) was identified in the sodium voltage-gated channel alpha subunit 1 gene () coding region. The variant co-segregated with the GEFSP phenotype in this family, and it was predicted as disease-causing by multiple programs, which was proposed as the genetic cause of GEFSP, further genetically diagnosed as GEFSP2. These findings expand the genetic and phenotypic spectrum of GEFSP and should contribute to genetic diagnoses, personalized therapies, and prognoses.
伴有热性惊厥附加症的遗传性癫痫(GEFSP)是一种家族性癫痫综合征,其基因具有异质性,多数情况下以常染色体显性形式遗传。迄今为止,至少有七个基因被报道与GEFSP相关。本研究旨在通过全外显子组测序、桑格测序和预测,鉴定一个患有GEFSP的中国土家族家族中的致病变异。在编码区的钠电压门控通道α亚基1基因()中鉴定出一个杂合错义变异c.5725A>G(p.T1909A)。该变异与该家族中的GEFSP表型共分离,并且通过多个程序预测为致病变异,被认为是GEFSP的遗传病因,进一步基因诊断为GEFSP2。这些发现扩展了GEFSP的遗传和表型谱,应为基因诊断、个性化治疗和预后提供帮助。