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首页> 外文期刊>Molecular medicine reports >Prevalence and range of GJB2 and SLC26A4 mutations in patients with autosomal recessive non-syndromic hearing loss
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Prevalence and range of GJB2 and SLC26A4 mutations in patients with autosomal recessive non-syndromic hearing loss

机译:常染色体隐性非综合征性聋的患者中GJB2和SLC26A4突变的发生率和范围

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The frequency and distribution of genetic mutations that cause deafness differ significantly according to ethnic group and region. Zhejiang is a province in the southeast of China, with an exceptional racial composition of the population caused by mass migration in ancient China. The purpose of the present study was to investigate the prevalence and spectrum of gap junction-? (GJB2), solute carrier family 26 (anion exchanger) member 4 (SLC26A4) and GJB3 mutations in patients with autosomal recessive non-syndromic hearing loss (ARNHL) in this area. A total of 176 unrelated pediatric patients with ARNHL were enrolled in the study. A genomic DNA sample was extracted from the peripheral blood. Polymerase chain reaction was employed, and the products were sequenced to screen for mutations in GJB2. In addition, a SNaPshot sequencing method was utilized to detect four hotspot mutations in SLC26A4 (IVS7-2A>G and c.2168A>G) and GJB3 (c.538C>T and c.547G>A). All patients were subjected to a temporal bone computed tomography scan to identify enlarged vestibular aqueducts (EVA). In total, 14 different mutations, including two new mutations (p.W44L and p.D66N) of GJB2, were detected. The most common pathogenic mutation of GJB2 was c.235delC (15.1%), followed by c.176-191del16 (1.7%), c.299-300delAT (1.7%), c.508-511dup (0.85%) and c.35delG (0.28%) of the total alleles. Mutation analysis of SLC26A4 demonstrated that 13.6% (24/176) of patients carried at least one mutant allele. The patients with EVA (84.2%) had SLC26A4 mutations, and 31% had homozygous mutations. Only one patient carried a heterozygous mutation of GJB3 (c.538C>T). Compared with the other regions of China, in the present population cohort, the prevalence and spectrum of mutations in GJB2 was unique, and in patients with EVA the frequency of a homozygous mutation in SLC26A4 was significantly lower. These findings may be of benefit in genetic counseling and risk assessment for families from this area of China.
机译:导致耳聋的遗传突变的频率和分布因种族和地区而异。浙江是中国东南部的一个省,由于中国古代的大规模迁徙,其人口构成具有特殊的种族特征。本研究的目的是研究间隙连接的发生率和光谱。 (GJB2),溶质载体家族26(阴离子交换剂)成员4(SLC26A4)和该区域常染色体隐性非综合征性非综合征性听力损失(ARNHL)患者的GJB3突变。本研究共纳入176名与ARNHL无关的儿科患者。从外周血中提取基因组DNA样品。使用聚合酶链反应,并对产物进行测序以筛选GJB2中的突变。此外,利用SNaPshot测序方法检测SLC26A4(IVS7-2A> G和c.2168A> G)和GJB3(c.538C> T和c.547G> A)中的四个热点突变。所有患者均接受颞骨计算机断层扫描,以确认前庭输水管(EVA)增大。总共检测到14种不同的突变,包括GJB2的两个新突变(p.W44L和p.D66N)。 GJB2最常见的致病突变是c.235delC(15.1%),其次是c.176-191del16(1.7%),c.299-300delAT(1.7%),c.508-511dup(0.85%)和c。总等位基因的35delG(0.28%)。 SLC26A4的突变分析表明13.6%(24/176)的患者携带至少一个突变等位基因。 EVA患者(84.2%)具有SLC26A4突变,而31%患者具有纯合突变。仅一名患者携带GJB3的杂合突变(c.538C> T)。与中国其他地区相比,在目前的人群队列中,GJB2突变的发生率和频谱是独特的,并且在患有EVA的患者中,SLC26A4的纯合突变频率明显更低。这些发现可能对中国这一地区家庭的遗传咨询和风险评估有益。

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