全外显子组测序在一个汉族牛头综合征家族中检测到一种新的AIFM1变异。

IF 2.7 3区 生物学 Hereditas Pub Date : 2023-05-12 DOI:10.1186/s41065-023-00282-z
Chenyu Wang, Zhaojing Lin, ZhuangZhuang Yuan, Tieyu Tang, Liangliang Fan, Yihui Liu, Xuan Wu
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引用次数: 0

摘要

charco - marie - tooth病(CMT)是一种遗传性周围神经病变,以进行性远端感觉减退和肌萎缩为特征。CMT具有X连锁隐性遗传的特点。凋亡诱导因子线粒体相关-1 (AIFM1)是伴有或不伴有小脑性共济失调的x连锁隐性沙克-玛丽-图斯病(CMTX4)的主要致病基因,也称为Cowchock综合征。在这项研究中,我们招募了一个来自中国东南地区的CMTX家族,并鉴定出一种新的AIFM1变异(NM_004208.3: c.931C>G;p.L311V)采用全外显子测序技术。我们的研究结果也可能对遗传咨询、体外受精胚胎的胚胎筛选和产前遗传诊断有用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Whole-exome sequencing detected a novel AIFM1 variant in a Han-Chinese family with Cowchock syndrome.

Charcot-Marie-Tooth disease(CMT) is a hereditary peripheral neuropathy, characterized by progressive distal hypoesthesia and amyotrophia. CMT is characterized by an X- linked recessive inheritance pattern. The apoptosis-inducing factor mitochondria associated-1 (AIFM1) is the main pathogenic gene of the X-linked recessive Charcot-Marie-Tooth disease-4 with or without cerebellar ataxia (CMTX4), also known as Cowchock syndrome. In this study, we enrolled a family with CMTX from the southeast region of China and identified a novel AIFM1 variant (NM_004208.3: c.931C>G; p.L311V) using whole exon sequencing technology. The results of our study may also be useful for genetic counseling, embryo screening of in vitro fertilization embryos, and prenatal genetic diagnosis.

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来源期刊
Hereditas
Hereditas Biochemistry, Genetics and Molecular Biology-Genetics
CiteScore
3.80
自引率
3.70%
发文量
0
期刊介绍: For almost a century, Hereditas has published original cutting-edge research and reviews. As the Official journal of the Mendelian Society of Lund, the journal welcomes research from across all areas of genetics and genomics. Topics of interest include human and medical genetics, animal and plant genetics, microbial genetics, agriculture and bioinformatics.
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