[osbpl2相关的常染色体显性听力损失:一个家族分析和文献综述]。

Q3 Medicine
X N Gu, S S Huang, X G Li, J Y Yang, Y Y Yuan
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引用次数: 0

摘要

回顾性分析了2022年6月至2025年2月在解放军总医院遗传性听力损失分子诊断中心通过全外显子组测序确定由OSBPL2基因变异引起的中国听力损失家庭。同时,检索PubMed和CNKI数据库(2014-2025)中与OSBPL2相关的耳聋文献,分析OSBPL2基因的基因型和表型。在607个耳聋家庭中,只有1个(0.16%)新的移码变异(影响氨基酸53,p.Gln53),表现为双侧、对称、迟发性、进行性感音神经性听力损失,从青春期晚期的高频开始,逐渐累及所有频率。该患者与先前报道的6个家族和1例散发病例在基因型和表型上表现出高度一致性。目前的研究结果表明,OSBPL2变异引起的常染色体显性非综合征性听力损失67 (DFNA67)是罕见的,主要是移码变异,并且可以重新发生,其中p.Gln53是突变热点。因此,对于以高频开始且表型相对统一的进行性感音神经性听力损失个体,应考虑进行OSBPL2基因检测。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[OSBPL2-related autosomal dominant hearing loss: a family analysis and literature review].

Chinese families with hearing loss definitively attributed to OSBPL2 gene variation via whole-exome sequencing at the Molecular Diagnostic Center for Hereditary Hearing Loss, PLA General Hospital from June 2022 to February 2025 were retrospectively analyzed. Meanwhile, a review of OSBPL2-related deafness literature from PubMed and CNKI databases (2014-2025) was performed to analyze the genotype and phenotype of OSBPL2 gene. Among 607 families with deafness, there was only one (0.16%) novel de novo frameshift variation (affecting amino acid 53, p.Gln53), presenting with bilateral, symmetric, late-onset, progressive sensorineural hearing loss starting with high frequencies during late adolescence and gradually involving all frequencies. This patient demonstrated high consistency in genotype and phenotype with six previously reported families and one sporadic case. The current findings reveal that OSBPL2 variants-caused autosomal dominant nonsyndromic hearing loss 67 (DFNA67) is rare, predominantly frameshift variations, and can occur de novo, with p.Gln53 as a mutation hotspot. Therefore, for individuals with progressive sensorineural hearing loss starting with high frequencies and having relatively uniform phenotype, genetic testing for OSBPL2 should be considered.

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来源期刊
Zhonghua yi xue za zhi
Zhonghua yi xue za zhi Medicine-Medicine (all)
CiteScore
0.80
自引率
0.00%
发文量
400
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