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Clin Med Insights Case Rep:感觉神经性耳聋患者中MYO15A新剪接变异位点报道和MYO15A变异谱分析

2019-10-07 AlexYang MedSci原创

常染色体隐性非综合征听力损失(ARNSHL)是一种遗传性的杂合感觉障碍,在新生儿中的发生率为1.4:1000。在ARNSHL患者中,已经报道了不少于60个基因与其有关,并且包括了MYO15A基因。最近,有研究人员通过临床外显子组测序鉴定和Sanger测序确认,报道了MYO15A基因中的一个新的变异。研究对象是一名22岁患有先天性非综合症感觉神经性耳聋的女性,其父母为近亲F=1/16,临床调查排除了

常染色体隐性非综合征听力损失(ARNSHL)是一种遗传性的杂合感觉障碍,在新生儿中的发生率为1.4:1000。在ARNSHL患者中,已经报道了不少于60个基因与其有关,并且包括了MYO15A基因。

最近,有研究人员通过临床外显子组测序鉴定和Sanger测序确认,报道了MYO15A基因中的一个新的变异。研究对象是一名22岁患有先天性非综合症感觉神经性耳聋的女性,其父母为近亲F=1/16,临床调查排除了变形特征。GJB2和GJB6基因的Sanger测序表明为阴性。之后,研究人员对其进行了临床外显子组测序。研究发现,在MYO15A基因中发现了一个新的纯和变异(c.9611_9612+8delTGGTGAGCAT),该变异引起了读码框在3204位密码子重新开始。研究人员利用Sanger测序确认了该变异并且其父母中均为杂合。

最后,研究人员指出,他们的结果表明了纯合MYO15A变异(c.9611_9612+8delTGGTGAGCAT)是一个致病性变异,该变异位点在任何数据库中还没有,因此是新的致病性变异。

原始出处:


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    2020-01-19 charl1234567
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    2019-10-09 yaanren
  9. 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