Beheshtian, M. and Babanejad, M. and Azaiez, H. and Bazazzadegan, N. and Kolbe, D. and Sloan-Heggen, C. and Arzhangi, S. and Booth, K. and Mohseni, M. and Frees, K. and Azizi, M.H. and Daneshi, A. and Farhadi, M. and Kahrizi, K. and Smith, R.J.H. and Najmabadi, H. (2016) Heterogeneity of hereditary hearing loss in Iran: A comprehensive review. Archives of Iranian Medicine, 19 (10). pp. 724-732.
Full text not available from this repository.Abstract
A significant contribution to the causes of hereditary hearing impairment comes from genetic factors. More than 120 genes and 160 loci have been identified to be involved in hearing impairment. Given that consanguine populations are more vulnerable to most inherited diseases, such as hereditary hearing loss (HHL), the genetic picture of HHL among the Iranian population, which consists of at least eight eth¬nic subgroups with a high rate of intermarriage, is expected to be highly heterogeneous. Using an electronic literature review through vari¬ous databases such as PubMed, MEDLINE, and Scopus, we review the current picture of HHL in Iran. In this review, we present more than 39 deafness genes reported to cause non-syndromic HHL in Iran, of which the most prevalent causative genes include GJB2, SLC26A4, MYO15A, and MYO7A. In addition, we highlight some of the more common genetic causes of syndromic HHL in Iran. These results are of importance for further investigation and elucidation of the molecular basis of HHL in Iran and also for developing a national diagnostic tool tailored to the Iranian context enabling early and efficient diagnosis ofhereditary hearing impairment. © 2016, Academy of Medical Sciences of I.R. Iran. All rights reserved.
| Item Type: | Article |
|---|---|
| Additional Information: | cited By 2 |
| Depositing User: | eprints admin |
| Date Deposited: | 08 Jul 2018 03:03 |
| Last Modified: | 08 Jul 2018 03:03 |
| URI: | http://eprints.iums.ac.ir/id/eprint/3210 |
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