Genetic Background of Congenital Hearing Loss.
- Author:
Seung Ha OH
1
;
Jae Jin SONG
Author Information
1. Department of otorhinolaryngology, Seoul National University College of Medicine, Korea. shaoh@snu.ac.kr
- Publication Type:Review
- Keywords:
Congenital hearing loss;
Genetics
- MeSH:
Ear, Inner;
Genes, Mitochondrial;
Genetic Counseling;
Hearing;
Hearing Loss;
Humans
- From:Journal of Genetic Medicine
2009;6(1):8-24
- CountryRepublic of Korea
- Language:Korean
-
Abstract:
Understanding the genetic background of hearing loss is important since almost 50% of the cases of profound hearing loss are caused by genetic factors. Until now, more than 150 causative genes have been identified. In this review, classification of genetic hearing loss (syndromic versus non-syndromic, recessive versus dominant, X-linked and mitochondrial), pitfalls in elucidating causative genes, anatomy of the inner ear, introduction of the most common syndromic hearing loss, introduction of the most common non-syndromic hearing loss-causing genes, mitochondrial and multifactorial hearing losses were discussed. Moreover, clinical approaches to the patients with hereditary hearing loss and genetic counseling were also explained briefly. Finally, future directions of the hereditary hearing loss research in Korean population were presented.
