Literature DB >> 10729800

Hereditary sensorineural hearing loss of unknown cause involving mitochondrial DNA 1555 mutation.

S Iwasaki1, Y Tamagawa, S Ocho, T Hoshino, K Kitamura.   

Abstract

We report on a family with maternally inherited sensorineural hearing loss, in which no history of aminoglycoside injection and no other specific etiology could be identified in any member. A 1555 A-to-G mutation of mitochondrial DNA was found in all members demonstrating hearing loss. The hearing in the propositus and his sister was severely impaired at a younger age than that in the mother. This case suggests that the 1555 point mutation of mitochondrial DNA has potential to promote inherited nonsyndromic hearing loss without any known etiology. Copyright 2000 S. Karger AG, Basel

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Year:  2000        PMID: 10729800     DOI: 10.1159/000027725

Source DB:  PubMed          Journal:  ORL J Otorhinolaryngol Relat Spec        ISSN: 0301-1569            Impact factor:   1.538


  3 in total

1.  Reduction of Cellular Expression Levels Is a Common Feature of Functionally Affected Pendrin (SLC26A4) Protein Variants.

Authors:  Vanessa C S de Moraes; Emanuele Bernardinelli; Nathalia Zocal; Jhonathan A Fernandez; Charity Nofziger; Arthur M Castilho; Edi L Sartorato; Markus Paulmichl; Silvia Dossena
Journal:  Mol Med       Date:  2016-01-04       Impact factor: 6.354

2.  [Mitochondrial A1555G mutation. Molecular genetic diagnosis in sporadic cases of non-syndromic hearing impairment].

Authors:  S Kupka; B Bodden-Kamps; M Baur; H P Zenner; M Pfister
Journal:  HNO       Date:  2004-11       Impact factor: 1.284

3.  Contribution of the GSTP1 c.313A>G variant to hearing loss risk in patients exposed to platin chemotherapy during childhood.

Authors:  P H P Liberman; M V S Goffi-Gomez; C Schultz; P L Jacob; C A A de Paula; E L Sartorato; G T Torrezan; E N Ferreira; D M Carraro
Journal:  Clin Transl Oncol       Date:  2018-10-25       Impact factor: 3.405

  3 in total

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