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机构地区:[1]浙江省绍兴市妇幼保健院,浙江312000 [2]杭州华大基因研究中心,浙江310004
出 处:《中国优生与遗传杂志》2014年第10期34-35,共2页Chinese Journal of Birth Health & Heredity
基 金:浙江省公益性技术应用研究计划项目(2013C33213)
摘 要:目的探讨新生儿听力与耳聋易感基因联合的必要性。方法应用飞行时间质谱技术,对2396名新生儿在听力筛查的同时,进行GJB2、GJB3、线粒体rRNA、SLC26A4 4个常见耳聋易感基因20个热点突变位点的检测。结果 2396例新生儿中,检出耳聋基因突变113例,阳性率47.16‰,其中致病突变14例,阳性率5.84‰,分别为GJB2 235delC纯合突变1例,GJB3 38C→T杂合突变6例和547 G→A杂合突变4例,线粒体rRNA 1555A→G纯合突变3例;杂合突变99例,阳性率41.32‰。确诊听力损失7例,其中3例耳聋基因检测阳性,分别为GJB2 235delC纯合突变、GJB2 235delC杂合突变和GJB3538C→T杂合突变。结论新生儿听力和耳聋易感基因联合筛查,有助早期发现与遗传相关的迟发性耳聋,预防药物性耳聋,应倡导新生儿听力与聋病易感基因联合筛查。Objective: To investigate the importance and necessity of newborn hearing screening combined with testing deafness predisposing genes. Method: Detecting the predisposing genes of GJB, GJB, SrRNA, SLCA including the hot spot mutations for newborns by MALDI-TOF. The result of hearing screening combined with testing deafness predisposing genes as experimental group, and the heating screening result as control group. Result: cases were found with deafness gene mutations among the newborns, The positive rate was. %, and cases are pathogenic mutation (is GJB delC homozygous mutation, are GJB C → T heterozygous mutation, are GJB G→ A heterozygous mutation, are S rRNAA→G homozygous mutation) , the ratio was.%; cases were diagnosed with heating loss, the incidence rate was.%o, and of them were GJB delC homozygous mutant, GJB delC heterozygous mutation and GJB C→T heterozygous mutation respectively. Conclusion: The newborn hearing screening combined with testing deafness predisposing genes can improve the detection rate of hearing loss/disease, especially for the genetic related late-onset deafness and drug poisoning deafness that can be found early. So the newborns should carry out universal hearing screening combined with testing deafness predisposing genes.
分 类 号:R764.43[医药卫生—耳鼻咽喉科]
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