The Analysis of GJB2, GJB3, and GJB6 Gene Mutations in Patients with Hereditary Non-Syndromic Hearing Loss Living in Sivas

• Published in: The journal of international advanced otology 2019-12, Vol.15 (3), p.373-378
• Main Authors: Kucuk Kurtulgan, Hande, Altuntas, Emine Elif, Yildirim, Malik Ejder, Ozdemir, Ozturk, Bagci, Binnur, Sezgin, Ilhan
• Format: Article
• Language: English
• Subjects: Adolescent; Adult; Aged; Analysis; Care and treatment; Child; Child, Preschool; Congenital diseases; Connexin 30 - genetics; Connexins - genetics; Consanguinity; Deoxyribonucleic acid; DNA; EDTA; Female; Gene Frequency; Gene mutation; Genes; Genetic aspects; Genetic counseling; Genetic disorders; Genetic research; Genotype; Health aspects; Hearing loss; Hearing Loss, Sensorineural - genetics; Hearing protection; Heterozygote; Homozygote; Humans; Male; Medical genetics; Medical screening; Middle Aged; Mutation; Original; Otolaryngology; Rehabilitation; Studies; Turkey; Young Adult
• ISSN: 1308-7649; 2148-3817
• DOI: 10.5152/iao.2019.5401

The aim of the present study was to investigate the presence of GJB2, GJB3, and GJB6 gene mutations in non-syndromic sensorineural hearing loss (NSHL) cases living in Sivas region, to provide appropriate genetic counseling for cases who were found to have mutation, and to contribute to decrease the frequency of mutant allele in the next generation and plan treatment and rehabilitation with early diagnosis. The study included 53 unrelated cases that were diagnosed with congenital NSHL between June 2009 and March 2010. Multiplex ligation-dependent probe amplification method was used for genotyping of GJB2, GJB3, and GJB6 gene mutations. Heterozygous 35delG variant was determined in 1.9% (n=1) of cases, homozygous 35delG in 15.1% (n=8), heterozygous IVS1+1G>A mutation in 1.9% (n=1), compound heterozygous in 3.8% (n=2), and homozygous IVS1+1G>A variant in 3.8% (n=2). None of the cases had mutation in GJB3 and GJB6 genes. Mutated allele frequencies in the present study were found to be 17.9% for 35delG and 6.6% for IVS1+1G>A. The present study showed that 35delG mutation is the most common variant in the Sivas region, and that IVS1+1G>A mutation should be investigated in hearing loss. Another result of the present study was that genetic analyzes would allow early diagnosis of hearing impairments particularly when infants whose parents have consanguinity do not pass the newborn hearing screening.