Literature DB >> 14604828

The genetic bases for syndromic and nonsyndromic deafness among Jews.

Tamar Ben-Yosef1, Thomas B Friedman.   

Abstract

There are hundreds of different mutated genes associated with hearing loss. However, recent findings indicate that a large proportion of both syndromic and nonsyndromic forms of deafness in some Jewish populations is caused by a small number of founder mutations. This review is focused on genetic disorders such as nonsyndromic deafness, Usher syndrome and Alport syndrome, in which hearing loss is a major part of the phenotype and in which the underlying prevalent founder mutations have been recently identified in different Jewish populations. These and other examples of common mutations within a distinct population allow for sensitive and specific use of genetic testing for carrier screening and diagnosis, and are an impetus for development of therapeutic strategies.

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Year:  2003        PMID: 14604828     DOI: 10.1016/j.molmed.2003.09.004

Source DB:  PubMed          Journal:  Trends Mol Med        ISSN: 1471-4914            Impact factor:   11.951


  3 in total

1.  The contribution of GJB2 mutations to slight or mild hearing loss in Australian elementary school children.

Authors:  H-H M Dahl; S E Tobin; Z Poulakis; F W Rickards; X Xu; L Gillam; J Williams; K Saunders; B Cone-Wesson; M Wake
Journal:  J Med Genet       Date:  2006-07-13       Impact factor: 6.318

Review 2.  The genetic bases for non-syndromic hearing loss among Chinese.

Authors:  Xiao Mei Ouyang; Denise Yan; Hui Jun Yuan; Dai Pu; Li Lin Du; Don Yi Han; Xue Zhong Liu
Journal:  J Hum Genet       Date:  2009-02-06       Impact factor: 3.172

Review 3.  The genetic and phenotypic landscapes of Usher syndrome: from disease mechanisms to a new classification.

Authors:  Sedigheh Delmaghani; Aziz El-Amraoui
Journal:  Hum Genet       Date:  2022-03-30       Impact factor: 5.881

  3 in total

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