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全外显子组测序是遗传性周围神经病的一种有价值的诊断工具:来自 50 个家族的队列研究结果。

Whole-exome sequencing is a valuable diagnostic tool for inherited peripheral neuropathies: Outcomes from a cohort of 50 families.

机构信息

Children's Hospital of Eastern Ontario Research Institute, University of Ottawa, Ottawa, Canada.

Department of Genetics, Children's Hospital of Eastern Ontario, Ottawa, Canada.

出版信息

Clin Genet. 2018 Feb;93(2):301-309. doi: 10.1111/cge.13101. Epub 2017 Dec 12.

DOI:10.1111/cge.13101
PMID:28708278
Abstract

The inherited peripheral neuropathies (IPNs) are characterized by marked clinical and genetic heterogeneity and include relatively frequent presentations such as Charcot-Marie-Tooth disease and hereditary motor neuropathy, as well as more rare conditions where peripheral neuropathy is associated with additional features. There are over 250 genes known to cause IPN-related disorders but it is estimated that in approximately 50% of affected individuals a molecular diagnosis is not achieved. In this study, we examine the diagnostic utility of whole-exome sequencing (WES) in a cohort of 50 families with 1 or more affected individuals with a molecularly undiagnosed IPN with or without additional features. Pathogenic or likely pathogenic variants in genes known to cause IPN were identified in 24% (12/50) of the families. A further 22% (11/50) of families carried sequence variants in IPN genes in which the significance remains unclear. An additional 12% (6/50) of families had variants in novel IPN candidate genes, 3 of which have been published thus far as novel discoveries (KIF1A, TBCK, and MCM3AP). This study highlights the use of WES in the molecular diagnostic approach of highly heterogeneous disorders, such as IPNs, places it in context of other published neuropathy cohorts, while further highlighting associated benefits for discovery.

摘要

遗传性周围神经病 (IPN) 的特征是明显的临床和遗传异质性,包括相对常见的表现,如夏科-马里-图思病和遗传性运动神经病,以及更罕见的情况下,周围神经病与其他特征相关。已知有超过 250 个基因可导致 IPN 相关疾病,但据估计,约有 50%的受影响个体未获得分子诊断。在这项研究中,我们检查了全外显子组测序 (WES) 在一组 50 个有 1 个或多个分子上未诊断的 IPN 伴有或不伴有其他特征的个体的家族中的诊断效用。在 24%(12/50)的家族中发现了已知导致 IPN 的基因中的致病性或可能致病性变异。另有 22%(11/50)的家族在 IPN 基因中携带序列变异,其意义尚不清楚。另外 12%(6/50)的家族在新的 IPN 候选基因中有变异,其中 3 个迄今已被发表为新发现(KIF1A、TBCK 和 MCM3AP)。这项研究强调了 WES 在高度异质性疾病(如 IPN)的分子诊断方法中的应用,将其置于其他已发表的神经病队列的背景下,同时进一步强调了发现相关的益处。

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