Analysis common gene mutation spots of 127 non-syndromic deafness natients in Guangxi Drovince.
- Author:
Shuixia LIU
;
Liang XU
;
Bowen CHEN
;
Min LIU
;
Shenghong QU
;
Jianping LIANG
;
Fengzhu TANG
;
Min SHI
;
Lu PENG
;
Yan JING
;
Fengti LI
;
Youqiong LIANG
- Publication Type:Journal Article
- MeSH:
China;
Connexin 26;
Connexins;
genetics;
DNA Mutational Analysis;
Deafness;
genetics;
Heterozygote;
Homozygote;
Humans;
Membrane Transport Proteins;
genetics;
Mutation;
Oligonucleotide Array Sequence Analysis;
Polymerase Chain Reaction;
RNA, Ribosomal;
genetics;
Sulfate Transporters
- From:
Journal of Clinical Otorhinolaryngology Head and Neck Surgery
2015;29(22):1954-1958
- CountryChina
- Language:Chinese
-
Abstract:
OBJECTIVE:To investigate the mutation characteristics of common deafness gene from 127 non-syndromic hearing loss patients in Guangxi province.
METHOD:Deafness-related gene mutations detection kit was used to detect 15 mutation sites in four deafness-associated genes, and a total of 127 hearing impaired patients were tested. The samples that could not be diagnosed with DNA microarray were subjected to PCR and sequenced to detect other mutations.
RESULT:Among the 127 patients with non-syndromic deafness, the total mutation rate is 8.66% (11/127), including GJB2 235delC homozygous in 3 cases (2.36%), 235delC single heterozygous mutation in 2 cases (1.57%), GJB2 235delC and 109 A > G mutations in 2 cases (1.57%); SLC26A4 1229C > T homozygous in 1 case (0.79%), IVS7-2A > G, IVS11 + 47T > C and 15448insC mutaion in 2 cases (1.57%); mitochondrial 12S rRNA gene mutations were not detected. The result indicates that GJB2 and SLC26A4 were the main genes in this study, and the mutation rate is significantly lower than the national average level. Three new mutations (SLC26A4 IVS11 + 47T > C,1548insC and GJB2 109A > G) were found. There may be rare mutations among sites or genes associated with deafness in Guangxi.
