Fertig Evan, Lincoln Anne, Martinuzzi Andrea, Mattson Richard H, Hisama Fuki M
Department of Neurology, Yale University School of Medicine, New Haven, CT, USA.
Neurology. 2003 May 27;60(10):1687-90. doi: 10.1212/01.wnl.0000063324.39980.4a.
Autosomal dominant partial epilepsy with auditory features (ADPEAF) is a rare idiopathic epilepsy syndrome caused by mutations in the leucine-rich, glioma-inactivated 1 (LGI1) gene. The authors report that molecular genetic studies in seven affected family members identified a novel F318C substitution that alters a highly conserved residue in a predicted repeat domain of unknown function. This report suggests that this domain may participate in the development of the ADPEAF phenotype.
常染色体显性遗传性听觉性癫痫(ADPEAF)是一种罕见的特发性癫痫综合征,由富含亮氨酸的胶质瘤失活1(LGI1)基因突变引起。作者报告称,对7名受影响家庭成员的分子遗传学研究发现了一种新的F318C替代突变,该突变改变了一个功能未知的预测重复结构域中一个高度保守的残基。该报告表明,这个结构域可能参与了ADPEAF表型的形成。