Genetic Etiology Study of Ten Chinese Families with Nonsyndromic Hearing Loss
Nonsyndromic hearing loss has been shown to have high genetic heterogeneity. In this report, we aimed to disclose the genetic causes of the subjects from the ten Chinese deaf families who did not have pathogenic common genes/mutation. Next-generation sequencing (NGS) of 142 known deafness genes was...
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| Main Authors: | , , , , , , |
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| Format: | Article |
| Language: | English |
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Wiley
2018-01-01
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| Series: | Neural Plasticity |
| Online Access: | http://dx.doi.org/10.1155/2018/4920980 |
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| author | Songqun Hu Feifei Sun Jie Zhang Yan Tang Jinhong Qiu Zhixia Wang Luping Zhang |
| author_facet | Songqun Hu Feifei Sun Jie Zhang Yan Tang Jinhong Qiu Zhixia Wang Luping Zhang |
| author_sort | Songqun Hu |
| collection | DOAJ |
| description | Nonsyndromic hearing loss has been shown to have high genetic heterogeneity. In this report, we aimed to disclose the genetic causes of the subjects from the ten Chinese deaf families who did not have pathogenic common genes/mutation. Next-generation sequencing (NGS) of 142 known deafness genes was performed in the probands of ten families followed by cosegregation analysis of all family members. We identified novel pathogenic variants in six families including p.D1806E/p.R1588W, p.R964W/p.R1588W, and p.G17C/p.G1449D in CDH23; p.T584M/p.D1939N in LOXHD1; p.P1225L in MYO7A; and p.K612X in EYA4. Sanger sequencing confirmed that these mutations segregated with the hearing loss of each family. In four families, no pathogenic variants were identified. Our study provided better understanding of the mutation spectrum of hearing loss in the Chinese population. |
| format | Article |
| id | doaj-art-c21047e131114385bbe046b6d59fc92d |
| institution | Kabale University |
| issn | 2090-5904 1687-5443 |
| language | English |
| publishDate | 2018-01-01 |
| publisher | Wiley |
| record_format | Article |
| series | Neural Plasticity |
| spelling | doaj-art-c21047e131114385bbe046b6d59fc92d2025-02-03T06:13:51ZengWileyNeural Plasticity2090-59041687-54432018-01-01201810.1155/2018/49209804920980Genetic Etiology Study of Ten Chinese Families with Nonsyndromic Hearing LossSongqun Hu0Feifei Sun1Jie Zhang2Yan Tang3Jinhong Qiu4Zhixia Wang5Luping Zhang6Department of Otolaryngology, Affiliated Hospital of Nantong University, Nantong, Jiangsu Province, ChinaDepartment of Otolaryngology, Affiliated Hospital of Nantong University, Nantong, Jiangsu Province, ChinaDepartment of Otolaryngology, Affiliated Hospital of Nantong University, Nantong, Jiangsu Province, ChinaDepartment of Otolaryngology, Affiliated Hospital of Nantong University, Nantong, Jiangsu Province, ChinaDepartment of Otolaryngology, Affiliated Hospital of Nantong University, Nantong, Jiangsu Province, ChinaDepartment of Otolaryngology, Affiliated Hospital of Nantong University, Nantong, Jiangsu Province, ChinaDepartment of Otolaryngology, Affiliated Hospital of Nantong University, Nantong, Jiangsu Province, ChinaNonsyndromic hearing loss has been shown to have high genetic heterogeneity. In this report, we aimed to disclose the genetic causes of the subjects from the ten Chinese deaf families who did not have pathogenic common genes/mutation. Next-generation sequencing (NGS) of 142 known deafness genes was performed in the probands of ten families followed by cosegregation analysis of all family members. We identified novel pathogenic variants in six families including p.D1806E/p.R1588W, p.R964W/p.R1588W, and p.G17C/p.G1449D in CDH23; p.T584M/p.D1939N in LOXHD1; p.P1225L in MYO7A; and p.K612X in EYA4. Sanger sequencing confirmed that these mutations segregated with the hearing loss of each family. In four families, no pathogenic variants were identified. Our study provided better understanding of the mutation spectrum of hearing loss in the Chinese population.http://dx.doi.org/10.1155/2018/4920980 |
| spellingShingle | Songqun Hu Feifei Sun Jie Zhang Yan Tang Jinhong Qiu Zhixia Wang Luping Zhang Genetic Etiology Study of Ten Chinese Families with Nonsyndromic Hearing Loss Neural Plasticity |
| title | Genetic Etiology Study of Ten Chinese Families with Nonsyndromic Hearing Loss |
| title_full | Genetic Etiology Study of Ten Chinese Families with Nonsyndromic Hearing Loss |
| title_fullStr | Genetic Etiology Study of Ten Chinese Families with Nonsyndromic Hearing Loss |
| title_full_unstemmed | Genetic Etiology Study of Ten Chinese Families with Nonsyndromic Hearing Loss |
| title_short | Genetic Etiology Study of Ten Chinese Families with Nonsyndromic Hearing Loss |
| title_sort | genetic etiology study of ten chinese families with nonsyndromic hearing loss |
| url | http://dx.doi.org/10.1155/2018/4920980 |
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