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两种检测方法对71例非综合征型耳聋患者基因检测结果的对比分析

韩锐 李林格 段玲 夏燕 陈俞

中国医药科学2016,Vol.6Issue(20):7-10,63,5.
中国医药科学2016,Vol.6Issue(20):7-10,63,5.

两种检测方法对71例非综合征型耳聋患者基因检测结果的对比分析

Contrast analysis of test results of two kinds of detection methods in 71 cases of non-syndromic deafness patients

韩锐 1李林格 2段玲 1夏燕 1陈俞2

作者信息

  • 1. 新疆医科大学第一附属医院产前诊断中心,新疆乌鲁木齐 830054
  • 2. 新疆医科大学第一附属医院耳鼻咽喉科,新疆乌鲁木齐 830054
  • 折叠

摘要

Abstract

Objective Using two different of methods to test 71 cases of non-syndromic deafness patients about the deafness gene, to provide more meaningful screening for clinic, to improve the deafness gene detection rate. Methods71 cases of non-syndromic deafness patients from July 2014 to December 2015 were selectrd as the study objects. Chip hybridization and multiple fluorescent PCR two different methods were used to test the 71 cases of non-comprehensive deafness patients about deafness gene, and SPSS17.0 software was used for the data analysis.Results There were significant diffience between the two kinds of methods for 71 cases of non-syndromic deafness patients (P<0.05). The deafness gene detection rate of chip hybridization method was 14.08% (10/71) , and the deafness gene detection rate of multiple fluorescent polymerase chain reaction (PCR) method was 30.98 (22/71) . Deafness gene's mutation site of the two methods was different, which led to a significant difference in detection rate. Conclusion Compared with chip detection method , increasing testing site in multiple fluorescent polymerase chain reaction ( PCR ) is meaningful for improving the clinical deafness gene screening rate .

关键词

耳聋/基因/突变/检出率

Key words

Deafness/Genes/Mutation/Detection rate

分类

医药卫生

引用本文复制引用

韩锐,李林格,段玲,夏燕,陈俞..两种检测方法对71例非综合征型耳聋患者基因检测结果的对比分析[J].中国医药科学,2016,6(20):7-10,63,5.

基金项目

新疆维吾尔自治区自然科学基金资助项目(2013211A102)。 ()

中国医药科学

2095-0616

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