Suppr超能文献

LARS2 变异体可在无明显听力损失的情况下表现为卵巢早衰。

LARS2 variants can present as premature ovarian insufficiency in the absence of overt hearing loss.

机构信息

CHU Rennes, Service de Biologie de la Reproduction-CECOS, F-35033, Rennes, France.

Univ Rennes, CHU Rennes, INSERM, EHESP, IRSET (Institut de Recherche en Santé, Environnement et Travail)-UMR_S 1085, F-35000, Rennes, France.

出版信息

Eur J Hum Genet. 2023 Apr;31(4):453-460. doi: 10.1038/s41431-022-01252-1. Epub 2022 Dec 1.

Abstract

Premature ovarian insufficiency (POI) affects 1 in 100 women and is a leading cause of female infertility. There are over 80 genes in which variants can cause POI, with these explaining only a minority of cases. Whole exome sequencing (WES) can be a useful tool for POI patient management, allowing clinical care to be personalized to underlying cause. We performed WES to investigate two French sisters, whose only clinical complaint was POI. Surprisingly, they shared one known and one novel likely pathogenic variant in the Perrault syndrome gene, LARS2. Using amino-acylation studies, we established that the novel missense variant significantly impairs LARS2 function. Perrault syndrome is characterized by sensorineural hearing loss in addition to POI. This molecular diagnosis alerted the sisters to the significance of their difficulty in following conversation. Subsequent audiology assessment revealed a mild bilateral hearing loss. We describe the first cases presenting with perceived isolated POI and causative variants in a Perrault syndrome gene. Our study expands the phenotypic spectrum associated with LARS2 variants and highlights the clinical benefit of having a genetic diagnosis, with prediction of potential co-morbidity and prompt and appropriate medical care, in this case by an audiologist for early detection of hearing loss.

摘要

卵巢早衰 (POI) 影响 1/100 的女性,是女性不孕的主要原因之一。有超过 80 个基因的变异可以导致 POI,但这些解释只占少数病例。外显子组测序 (WES) 可以成为 POI 患者管理的有用工具,使临床护理能够针对潜在病因进行个性化定制。我们对两名法国姐妹进行了 WES 研究,她们唯一的临床主诉是 POI。令人惊讶的是,她们在 Perrault 综合征基因 LARS2 中共享一个已知和一个新的可能致病变异。通过氨酰化研究,我们确定该新型错义变异显著损害了 LARS2 的功能。Perrault 综合征的特征除了 POI 外,还有感觉神经性听力损失。这一分子诊断使姐妹俩意识到她们在交谈中遇到困难的重要性。随后的听力学评估显示出双侧轻度听力损失。我们描述了首例表现为感知孤立性 POI 且与 Perrault 综合征基因中的致病变异相关的病例。我们的研究扩展了与 LARS2 变异相关的表型谱,并强调了遗传诊断的临床益处,可预测潜在的合并症,并及时提供适当的医疗护理,在这种情况下,通过听力学家早期发现听力损失。

相似文献

2
Expanding the genotypic spectrum of Perrault syndrome.扩展佩罗特综合征的基因型谱。
Clin Genet. 2017 Feb;91(2):302-312. doi: 10.1111/cge.12776. Epub 2016 Apr 1.
7
Perrault syndrome: Clinical report and retrospective analysis.佩罗特综合征:临床报告及回顾性分析。
Mol Genet Genomic Med. 2020 Oct;8(10):e1445. doi: 10.1002/mgg3.1445. Epub 2020 Aug 7.

引用本文的文献

4
Premature ovarian insufficiency.卵巢早衰。
Nat Rev Dis Primers. 2024 Sep 12;10(1):63. doi: 10.1038/s41572-024-00547-5.
8
2023 in the European Journal of Human Genetics.发表于《欧洲人类遗传学杂志》2023年刊。
Eur J Hum Genet. 2024 Feb;32(2):135-137. doi: 10.1038/s41431-024-01540-y.

本文引用的文献

4
Perrault syndrome: Clinical report and retrospective analysis.佩罗特综合征:临床报告及回顾性分析。
Mol Genet Genomic Med. 2020 Oct;8(10):e1445. doi: 10.1002/mgg3.1445. Epub 2020 Aug 7.
8
Aminoacyl-tRNA synthetases.氨酰-tRNA 合成酶。
RNA. 2020 Aug;26(8):910-936. doi: 10.1261/rna.071720.119. Epub 2020 Apr 17.

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