Literature DB >> 17428550

High carrier frequency of the GJB2 mutation (35delG) in the north of Iran.

Morteza Hashemzadeh Chaleshtori1, Effat Farrokhi, Mehrdad Shahrani, Soleiman Kheiri, Masoumeh Dolati, Laleh Hoghooghi Rad, Hamid Pour-Jafari, Keihan Ghatreh Samani, Katayoon Safa Chaleshtori, Andrew H Crosby.   

Abstract

OBJECTIVE: Mutations in the GJB2 gene are a major cause of autosomal recessive and sporadic non-syndromic hearing loss in many populations. A single mutation of this gene (35delG) accounts for approximately 70% of mutations in Caucasians with a carrier frequency of 2-4% in Europe. This study aims to determine the rate of 35delG carrier frequency in Iran.
METHODS: Genomic DNA was extracted from a total of 550 unaffected unrelated subjects from 4 provinces of Iran following the standard phenol chloroform procedure. The one base pair deletion (35delG) was analysed using a nested PCR procedure; 35delG mutation carriers were subsequently confirmed by sequence analysis. Moreover, using the Binomial probability distribution, we compared the 35delG carrier frequency of Iranian population with the various Middle Eastern and overall European populations.
RESULTS: Of the four populations studied, we found a high carrier frequency of 2.8% in Gilan province in the north of Iran. The overall 35delG carrier frequency was found to be 1.25% in the populations studied (our present and previous data) which is similar to the overall 35delG carrier frequency detected in Middle Eastern populations, but Significantly lower than that identified in European populations.

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Year:  2007        PMID: 17428550     DOI: 10.1016/j.ijporl.2007.02.005

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


  6 in total

1.  Conditional deletion of pejvakin in adult outer hair cells causes progressive hearing loss in mice.

Authors:  Suzan L Harris; Marcin Kazmierczak; Tina Pangršič; Prahar Shah; Nadiya Chuchvara; Alonso Barrantes-Freer; Tobias Moser; Martin Schwander
Journal:  Neuroscience       Date:  2017-01-09       Impact factor: 3.590

2.  Did the GJB2 35delG mutation originate in Iran?

Authors:  Vahideh Norouzi; Hiva Azizi; Zohreh Fattahi; Fatemehsadat Esteghamat; Niloofar Bazazzadegan; Carla Nishimura; Nooshin Nikzat; Khadijeh Jalalvand; Kimia Kahrizi; Richard J H Smith; Hossein Najmabadi
Journal:  Am J Med Genet A       Date:  2011-09-09       Impact factor: 2.802

3.  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

Review 4.  Genetics of Hearing Loss in North Iran Population: An Update of Spectrum and Frequency of GJB2 Mutations.

Authors:  Mahbobeh Koohiyan; Fatemeh Azadegan-Dehkordi; Farideh Koohian; Morteza Hashemzadeh-Chaleshtori
Journal:  J Audiol Otol       Date:  2019-06-27

5.  Mutations in GJB2 as Major Causes of Autosomal Recessive Non-Syndromic Hearing Loss: First Report of c.299-300delAT Mutation in Kurdish Population of Iran.

Authors:  Fatemeh Azadegan-Dehkordi; Tayyebe Bahrami; Maryam Shirzad; Gelareh Karbasi; Nasrin Yazdanpanahi; Effat Farrokhi; Mahbobeh Koohiyan; Mohammad Amin Tabatabaiefar; Morteza Hashemzadeh-Chaleshtori
Journal:  J Audiol Otol       Date:  2018-12-07

6.  Association of nuclear and mitochondrial genes with audiological examinations in Iranian patients with nonaminoglycoside antibiotics-induced hearing loss.

Authors:  Maryam Balali; Behnam Kamalidehghan; Mohammad Farhadi; Fatemeh Ahmadipour; Mahmoud Dehghani Ashkezari; Mohsen Rezaei Hemami; Hossein Arabzadeh; Masoumeh Falah; Goh Yong Meng; Massoud Houshmand
Journal:  Ther Clin Risk Manag       Date:  2016-01-28       Impact factor: 2.423

  6 in total

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