Literature DB >> 10219384

Sensorineural hearing loss and the 1555G mitochondrial DNA mutation.

T Hutchin1.   

Abstract

Recent studies have identified a mitochondrial DNA mutation (1555G) which causes sensorineural hearing loss (SNHL). In many cases deafness follows exposure to aminoglycoside antibiotics, the 1555G mutation sensitizing the inner ear to these drugs. The 50 cases reported to date are discussed, as are the possible mechanisms behind the pathogenesis of this mutation. This finding in families from a wide range of ethnic backgrounds suggests that the 1555G mutation is one of the more common genetic causes of SNHL and provides a fascinating example of how a genetic mutation interacts with an environmental factor with harmful effect.

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Year:  1999        PMID: 10219384     DOI: 10.1080/00016489950181927

Source DB:  PubMed          Journal:  Acta Otolaryngol        ISSN: 0001-6489            Impact factor:   1.494


  3 in total

Review 1.  [Mitochondrial hearing impairment. Background, genetic predisposition and possibilities for diagnosis].

Authors:  K Riemann; M Pfister; N Blin; S Kupka
Journal:  HNO       Date:  2004-06       Impact factor: 1.284

2.  The A1555G mutation in the 12S rRNA gene of human mtDNA: recurrent origins and founder events in families affected by sensorineural deafness.

Authors:  A Torroni; F Cruciani; C Rengo; D Sellitto; N López-Bigas; R Rabionet; N Govea; A López De Munain; M Sarduy; L Romero; M Villamar; I del Castillo; F Moreno; X Estivill; R Scozzari
Journal:  Am J Hum Genet       Date:  1999-11       Impact factor: 11.025

3.  Analysis of functional variants in mitochondrial DNA of Finnish athletes.

Authors:  Jukka Kiiskilä; Jukka S Moilanen; Laura Kytövuori; Anna-Kaisa Niemi; Kari Majamaa
Journal:  BMC Genomics       Date:  2019-10-29       Impact factor: 3.969

  3 in total

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