Shirkavand, Atefeh, Zeinali, Sirous, Mahdieh, Nejat, Bagherian, Hamideh, Sharafi Farzad, Maryam, Vahidi, Roghayeh, Kianfar, Soodeh, Ghahremani, Sahar, Asheri, Maryam, Raeisi, Marzieh, Zeinali, Zahra, Zafari, Zahra, Ghasemi, Akram, Zeinali, Sirous (2010). Investigation of connexin 26 mutations and three large deletions spanning connexin 30 in 63 Iranian families with autosomal recessive non-syndromic hearing loss. , 13(2), 23-32.
Atefeh Shirkavand; Sirous Zeinali; Nejat Mahdieh; Hamideh Bagherian; Maryam Sharafi Farzad; Roghayeh Vahidi; Soodeh Kianfar; Sahar Ghahremani; Maryam Asheri; Marzieh Raeisi; Zahra Zeinali; Zahra Zafari; Akram Ghasemi; Sirous Zeinali. "Investigation of connexin 26 mutations and three large deletions spanning connexin 30 in 63 Iranian families with autosomal recessive non-syndromic hearing loss". , 13, 2, 2010, 23-32.
Shirkavand, Atefeh, Zeinali, Sirous, Mahdieh, Nejat, Bagherian, Hamideh, Sharafi Farzad, Maryam, Vahidi, Roghayeh, Kianfar, Soodeh, Ghahremani, Sahar, Asheri, Maryam, Raeisi, Marzieh, Zeinali, Zahra, Zafari, Zahra, Ghasemi, Akram, Zeinali, Sirous (2010). 'Investigation of connexin 26 mutations and three large deletions spanning connexin 30 in 63 Iranian families with autosomal recessive non-syndromic hearing loss', , 13(2), pp. 23-32.
Shirkavand, Atefeh, Zeinali, Sirous, Mahdieh, Nejat, Bagherian, Hamideh, Sharafi Farzad, Maryam, Vahidi, Roghayeh, Kianfar, Soodeh, Ghahremani, Sahar, Asheri, Maryam, Raeisi, Marzieh, Zeinali, Zahra, Zafari, Zahra, Ghasemi, Akram, Zeinali, Sirous Investigation of connexin 26 mutations and three large deletions spanning connexin 30 in 63 Iranian families with autosomal recessive non-syndromic hearing loss. , 2010; 13(2): 23-32.

Investigation of connexin 26 mutations and three large deletions spanning connexin 30 in 63 Iranian families with autosomal recessive non-syndromic hearing loss

Pathobiology Reserach
Article 3, Volume 13, Issue 2, 2010, Pages 23-32    PDF (592.27 K)
Authors
Atefeh Shirkavand1; Sirous Zeinali* 2; Nejat Mahdieh3; Hamideh Bagherian4; Maryam Sharafi Farzad5; Roghayeh Vahidi5; Soodeh Kianfar5; Sahar Ghahremani5; Maryam Asheri5; Marzieh Raeisi5; Zahra Zeinali6; Zahra Zafari7; Akram Ghasemi8; Sirous Zeinali* 2
1M.Sc. Student, Department of Biology, Faculty of Sciences, Razi University, Kermanshah, Iran
2Associate Professor, Biotechnology Research Center, Pastuer Institute of Iran, Tehran, Iran
3Ph.D. Student, Department of Medical Genetics, Faculty of Medicine, Ilam University of Medical Sciences, Ilam, Iran
4M.D. and Genetic Counselor, Medical Genetics Laboratory of Dr. Zeinali, Kawsar's Human Genetics Research Center, Tehran, Iran
5B.Sc., Medical Genetics Laboratory of Dr. Zeinali, Kawsar's Human Genetics Research Center, Tehran, Iran
6M.D. Student, Faculty of Medicine, Iran university of Medical Sciences, Tehran, Iran
7M.Sc. Student, Department of Biology, Khatam University, Tehran, Iran
8M.Sc. Student, Department of Microbiology, Azad University of Jahrom, Fars, Iran
Abstract
Objective: Hearing loss is the most frequent neurosensory defect in human. Mutations in GJB2 and GJB6 are responsible for 50% of autosomal recessive non-syndromic hearing loss (ARNSHL) cases. Here we report on the frequencies of GJB2 and GJB6 mutations and three large deletions spanning the GJB6 gene including Del (GJB6-D13S1830), Del (GJB6-D13S1854) and a >920 kb deletion in patients affected by ARNSHL referred to Kawsar's Human Genetics Research Center.
Materials and Methods: In this study, 94 patients from 63 families with ARNSHL were investigated. Patient's homozygote for 35delG were screened and left out of the study and the remaining samples were analyzed by sequencing of GJB2 and GJB6 genes. Also the three large deletions spanning the GJB6 gene were analyzed by Real Time PCR
Results: In this study we found GJB2 mutations in 13 families (20.6%) out of 63. The 35delG mutation was the most common mutation in the studied population (61.5%). Other GJB2 mutations were delE120, R127H, W24X, and V37I. The heterozygous or negative cases for the GJB2 mutations were screened for mutation in the GJB6 gene by sequencing and no mutation was observed. Also, we checked the three large deletions in GJB6, we found no mutations.
Conclusion: Low frequency of mutations in the GJB2 gene implies that other genes may be involved in causing non-syndromic hearing loss in our country.
Keywords
PCR; GJB2; Non Syndromic Hearing Loss; population
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