Suppr超能文献

发作性共济失调相关基因的基因型-表型关系:MDSGene 系统综述。

Genotype-phenotype relations for episodic ataxia genes: MDSGene systematic review.

机构信息

Edmond J. Safra Program in Parkinson's Disease and the Morton and Gloria Shulman Movement Disorders Clinic, Toronto Western Hospital, Division of Neurology, University of Toronto, Toronto, Ontario, Canada.

Department of Neurology, Faculty of Medicine and Dentistry, University of Alberta, Edmonton, Alberta, Canada.

出版信息

Eur J Neurol. 2023 Oct;30(10):3377-3393. doi: 10.1111/ene.15969. Epub 2023 Jul 17.

Abstract

BACKGROUND

Most episodic ataxias (EA) are autosomal dominantly inherited and characterized by recurrent attacks of ataxia and other paroxysmal and non-paroxysmal features. EA is often caused by pathogenic variants in the CACNA1A, KCNA1, PDHA1, and SLC1A3 genes, listed as paroxysmal movement disorders (PxMD) by the MDS Task Force on the Nomenclature of Genetic Movement Disorders. Little is known about the genotype-phenotype correlation of the different genetic EA forms.

METHODS

We performed a systematic review of the literature to identify individuals affected by an episodic movement disorder harboring pathogenic variants in one of the four genes. We applied the standardized MDSGene literature search and data extraction protocol to summarize the clinical and genetic features. All data are available via the MDSGene protocol and platform on the MDSGene website (https://www.mdsgene.org/).

RESULTS

Information on 717 patients (CACNA1A: 491, KCNA1: 125, PDHA1: 90, and SLC1A3: 11) carrying 287 different pathogenic variants from 229 papers was identified and summarized. We show the profound phenotypic variability and overlap leading to the absence of frank genotype-phenotype correlation aside from a few key 'red flags'.

CONCLUSION

Given this overlap, a broad approach to genetic testing using a panel or whole exome or genome approach is most practical in most circumstances.

摘要

背景

大多数发作性共济失调(EA)为常染色体显性遗传,以复发性共济失调和其他阵发性及非阵发性特征为特征。EA 通常由 CACNA1A、KCNA1、PDHA1 和 SLC1A3 基因中的致病性变异引起,MDS 命名遗传运动障碍工作组将其列为阵发性运动障碍(PxMD)。对于不同遗传 EA 形式的基因型-表型相关性知之甚少。

方法

我们对文献进行了系统回顾,以确定患有发作性运动障碍且携带四个基因之一中的致病性变异的个体。我们应用标准化的 MDSGene 文献检索和数据提取方案来总结临床和遗传特征。所有数据均可通过 MDSGene 协议和 MDSGene 网站上的平台(https://www.mdsgene.org/)获得。

结果

从 229 篇论文中确定并总结了 717 名(CACNA1A:491、KCNA1:125、PDHA1:90 和 SLC1A3:11)携带 287 种不同致病性变异的患者的信息。我们展示了明显的表型变异性和重叠,导致除了少数关键“红旗”外,缺乏明显的基因型-表型相关性。

结论

鉴于这种重叠,在大多数情况下,使用面板或全外显子组或全基因组方法进行广泛的基因检测是最实用的。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验