Volume 2, Issue 1 (Int J Mol Cell Med 2013)                   Int J Mol Cell Med 2013, 2(1): 41-45 | Back to browse issues page

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1- Department of Genetic, Faculty of Science, ShahidChamran University of Ahwaz, Ahwaz, Iran. , mchalesh@yahoo.com
2- Department of Genetic, Faculty of Science, ShahidChamran University of Ahwaz, Ahwaz, Iran.
3- Cellular and Molecular Biology Research Center (CMBRC), Babol University of Medical Sciences, Babol, Iran.
4- Department of Biochemistry and Genetics, Falavarjan Branch, Islamic Azad University, Isfahan, Iran.
5- Department of Genetics, Faculty of Medicine, JundiShapur University of Medical Sciences, Ahwaz, Iran.
6- Department of Basic Sciences, Faculty of Veterinary Medicine, Shahrekord University, Shahrekord, Iran.
7- Department of Genetics, Faculty of Science, Shahrekord University, Shahrekord, Iran.
8- Cellular and Molecular Research Center, Shahrekord University of Medical Sciences, Shahrekord, Iran.
Abstract:   (14269 Views)
Hearing loss (HL) is the most frequent sensory defect affecting 1 in 1000 neonates. This can occur due to genetic or environmental causes or both. The genetic causes are very heterogenous and over 100 loci have been identified to cause autosomal recessive non - syndromic hearing loss (ARNSHL). The aim of this study was to determine the contribution of the LRTOMT gene mutations in causing ARNSHL. One hundred fifty seven pupils affected with ARNSHL from Azarbaijan Sharghi, Kordestan, Gilan and Golestan provinces, north and west of Iran, were ascertained. In this descriptive - laboratory study, the presence of LRTOMT mutations were initially checked using PCR – Single - strand conformation polymorphism (SSCP) and heteroduplex analysis (HA) strategy. Samples with shifted bands on the gel were confirmed by DNA sequencing method. The PCR-SSCP/HA and the subsequent direct DNA sequencing showed no mutation in the population studied. We conclude that LRTOMT mutations have no role in causing sporadic deafness in the studied population. Further studies on other populations and samples could clarify the exact role of LRTOMT mutations.
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Type of Study: Original Article | Subject: Genetics & Disease
Received: 2013/02/9 | Accepted: 2013/06/22 | Published: 2013/06/22

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