Suppr超能文献

一个家族性低钾周期性麻痹患者的钙通道基因突变

A novel mutation in the calcium channel gene in a family with hypokalemic periodic paralysis.

机构信息

Department of Neurology, Sakai Hospital Kinki University Faculty of Medicine, Sakai, Osaka, Japan.

出版信息

J Neurol Sci. 2011 Oct 15;309(1-2):9-11. doi: 10.1016/j.jns.2011.07.046. Epub 2011 Aug 19.

Abstract

Hypokalemic periodic paralysis (HypoPP) type 1 is an autosomal dominant disease caused by mutations in the Ca(V)1.1 calcium channel encoded by the CACNA1S gene. Only seven mutations have been found since the discovery of the causative gene in 1994. We describe a patient with HypoPP who had a high serum potassium concentration after recovery from a recent paralysis, which complicated the correct diagnosis. This patient and other affected family members had a novel mutation, p.Arg900Gly, in the CACNA1S gene.

摘要

低钾周期性麻痹(HypoPP)1 型是一种常染色体显性疾病,由编码 Ca(V)1.1 钙通道的 CACNA1S 基因突变引起。自 1994 年发现致病基因以来,仅发现了七种突变。我们描述了一位 HypoPP 患者,在最近一次麻痹恢复后血清钾浓度升高,这使正确诊断变得复杂。该患者和其他受影响的家庭成员在 CACNA1S 基因中存在新的突变 p.Arg900Gly。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验