Literature DB >> 22906306

Screening of OTOF mutations in Iran: a novel mutation and review.

Nejat Mahdieh1, Atefeh Shirkavand, Bahareh Rabbani, Mustafa Tekin, Bahman Akbari, Mohammad Taghi Akbari, Sirous Zeinali.   

Abstract

OBJECTIVE: Mutations in OTOF have been reported to cause nonsyndromic hearing loss in different populations. The purpose of this study is screening of OTOF mutations in Iranian population.
METHODS: Thirty-eight consanguineous families affected with autosomal recessive nonsyndromic hearing loss (ARNSHL) and negative for GJB2 or GJB6 mutations were screened by autozygosity mapping and Sanger sequencing to find OTOF mutations.
RESULTS: A novel homozygous frameshift mutation (c.1981dupG) was found to cause hearing loss in one family and no other OTOF variants were detected in the remaining families. The affected individuals were homozygous forp. D661GfsX2 causing defect in long isoform of otoferlin.
CONCLUSIONS: We conclude that OTOF mutations are not the major cause of ARNSHL in the Iranian population but still may play an important role in HL; therefore evaluation the OTOF gene is of concern.
Copyright © 2012 Elsevier Ireland Ltd. All rights reserved.

Entities:  

Mesh:

Substances:

Year:  2012        PMID: 22906306     DOI: 10.1016/j.ijporl.2012.07.030

Source DB:  PubMed          Journal:  Int J Pediatr Otorhinolaryngol        ISSN: 0165-5876            Impact factor:   1.675


  18 in total

Review 1.  Heterogeneity of Hereditary Hearing Loss in Iran: a Comprehensive Review.

Authors:  Maryam Beheshtian; Mojgan Babanejad; Hela Azaiez; Niloofar Bazazzadegan; Diana Kolbe; Christina Sloan-Heggen; Sanaz Arzhangi; Kevin Booth; Marzieh Mohseni; Kathy Frees; Mohammad Hossein Azizi; Ahmad Daneshi; Mohammad Farhadi; Kimia Kahrizi; Richard Jh Smith; Hossein Najmabadi
Journal:  Arch Iran Med       Date:  2016-10-01       Impact factor: 1.354

2.  GJB2 mutations in deaf population of Ilam (Western Iran): a different pattern of mutation distribution.

Authors:  Nejat Mahdieh; Hamdollah Mahmoudi; Soleiman Ahmadzadeh; Salar Bakhtiyari
Journal:  Eur Arch Otorhinolaryngol       Date:  2015-06-10       Impact factor: 2.503

3.  The natural history of OTOF-related auditory neuropathy spectrum disorders: a multicenter study.

Authors:  Ryan K Thorpe; Hela Azaiez; Peina Wu; Qiuju Wang; Lei Xu; Pu Dai; Tao Yang; G Bradley Schaefer; B Robert Peters; Kenny H Chan; Krista S Schatz; Joann Bodurtha; Nathaniel H Robin; Yoel Hirsch; Zuhair Abdalla Rahbeeni; Huijun Yuan; Richard J H Smith
Journal:  Hum Genet       Date:  2021-08-23       Impact factor: 5.881

4.  Evidence for genotype-phenotype correlation for OTOF mutations.

Authors:  Muzeyyen Yildirim-Baylan; Guney Bademci; Duygu Duman; Hatice Ozturkmen-Akay; Suna Tokgoz-Yilmaz; Mustafa Tekin
Journal:  Int J Pediatr Otorhinolaryngol       Date:  2014-03-28       Impact factor: 1.675

5.  Diversity of the causal genes in hearing impaired Algerian individuals identified by whole exome sequencing.

Authors:  Fatima Ammar-Khodja; Crystel Bonnet; Malika Dahmani; Sofiane Ouhab; Gaelle M Lefèvre; Hassina Ibrahim; Jean-Pierre Hardelin; Dominique Weil; Malek Louha; Christine Petit
Journal:  Mol Genet Genomic Med       Date:  2015-02-15       Impact factor: 2.183

6.  OTOF mutation screening in Japanese severe to profound recessive hearing loss patients.

Authors:  Yoh-ichiro Iwasa; Shin-ya Nishio; Hidekane Yoshimura; Yukihiko Kanda; Kozo Kumakawa; Satoko Abe; Yasushi Naito; Kyoko Nagai; Shin-ichi Usami
Journal:  BMC Med Genet       Date:  2013-09-22       Impact factor: 2.103

7.  Whole Exome Sequencing Reveals Homozygous Mutations in RAI1, OTOF, and SLC26A4 Genes Associated with Nonsyndromic Hearing Loss in Altaian Families (South Siberia).

Authors:  Alexander Y Сhurbanov; Tatiana M Karafet; Igor V Morozov; Valeriia Yu Mikhalskaia; Marina V Zytsar; Alexander A Bondar; Olga L Posukh
Journal:  PLoS One       Date:  2016-04-15       Impact factor: 3.240

8.  Genetic Linkage Analysis of DFNB3, DFNB9 and DFNB21 Loci in GJB2 Negative Families with Autosomal Recessive Non-syndromic Hearing Loss.

Authors:  Marjan Masoudi; Najmeh Ahangari; Ali Akbar Poursadegh Zonouzi; Ahmad Poursadegh Zonouzi; Azim Nejatizadeh
Journal:  Iran J Public Health       Date:  2016-05       Impact factor: 1.429

9.  Identification of a Novel MYO15A Mutation in a Chinese Family with Autosomal Recessive Nonsyndromic Hearing Loss.

Authors:  Hong Xia; Xiangjun Huang; Yi Guo; Pengzhi Hu; Guangxiang He; Xiong Deng; Hongbo Xu; Zhijian Yang; Hao Deng
Journal:  PLoS One       Date:  2015-08-26       Impact factor: 3.240

10.  A novel missense mutation in the C2C domain of otoferlin causes profound hearing impairment in an Omani family with auditory neuropathy.

Authors:  Nadia M Al-Wardy; Mohammed N Al-Kindi; Mazin J Al-Khabouri; Yahya Tamimi; Guy Van Camp
Journal:  Saudi Med J       Date:  2016-10       Impact factor: 1.484

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.