Epilepsy Research Centre, Department of Medicine, The University of Melbourne, Austin Health, Melbourne, Australia.
Epilepsy Res. 2013 Jan;103(1):97-100. doi: 10.1016/j.eplepsyres.2012.10.009. Epub 2012 Nov 20.
A homozygous SCN1B mutation was previously identified in a patient with early onset epileptic encephalopathy (EOEE) described as Dravet syndrome (DS) despite a more severe phenotype than DS. We investigated whether SCN1B mutations are a common cause of DS. Patients with DS who did not have a SCN1A sequencing mutation or copy number variation were studied. Genomic DNA was Sanger sequenced for mutations in the 6 exons of SCN1B. In 54 patients with DS recruited from four centres, no SCN1B mutations were identified. SCN1B mutation is not a common cause of DS.
先前在一名早发性癫痫性脑病(EOEE)患者中发现了一个 SCN1B 纯合突变,该患者的表型比 Dravet 综合征(DS)更为严重,被描述为 Dravet 综合征(DS)。我们研究了 SCN1B 突变是否是 DS 的常见原因。研究了没有 SCN1A 测序突变或拷贝数变异的 DS 患者。对 SCN1B 的 6 个外显子的基因突变进行了 Sanger 测序。在从四个中心招募的 54 名 DS 患者中,未发现 SCN1B 突变。SCN1B 突变不是 DS 的常见原因。