Literature DB >> 11558763

The DFNA10 phenotype.

E M De Leenheer1, P L Huygen, S Wayne, R J Smith, C W Cremers.   

Abstract

We present a detailed analysis of the DFNA10 phenotype based on data from 25 hearing-impaired persons coming from a large American pedigree segregating for deafness at the DFNA10 locus (chromosome 6q22.3-23.2). Cross-sectional analysis of air conduction threshold-on-age data from all available last-visit audiograms (linear regression analysis, age over 15 years) showed progression of hearing loss at a rate of 0.6 dB/y over all frequencies, with a flat to gently sloping age-corrected threshold of about 50 dB. The results were significant at 0.25, 4, and 8 kHz, but only if corrections for presbycusis were not included. Longitudinal threshold analysis performed in 1 case, covering ages 6 to 32 years, showed progression of hearing loss at a rate of 2 to 3 dB/y over 0.25 to 8 kHz. Nonlinear regression analysis was performed on phoneme discrimination scores with use of sigmoidal dose-response curves with variable slope. On the basis of these data, the hearing loss phenotype in this American DFNA10 family can be described as postlingual, initially progressive, and resulting, without the influence of presbycusis, in largely stable, flat sensorineural deafness.

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Year:  2001        PMID: 11558763     DOI: 10.1177/000348940111000910

Source DB:  PubMed          Journal:  Ann Otol Rhinol Laryngol        ISSN: 0003-4894            Impact factor:   1.547


  5 in total

1.  A comparative study of Eya1 and Eya4 protein function and its implication in branchio-oto-renal syndrome and DFNA10.

Authors:  Yuzhou Zhang; Boyd M Knosp; Mark Maconochie; Rick A Friedman; Richard J H Smith
Journal:  J Assoc Res Otolaryngol       Date:  2004-06-24

2.  Histopathology of nonsyndromic autosomal dominant midfrequency sensorineural hearing loss.

Authors:  Fayez Bahmad; Jennifer O'Malley; Lisbeth Tranebjaerg; Saumil N Merchant
Journal:  Otol Neurotol       Date:  2008-08       Impact factor: 2.311

3.  Sensorineural hearing loss and mild cardiac phenotype caused by an EYA4 mutation.

Authors:  Satoko Abe; Hidehiko Takeda; Shin-Ya Nishio; Shin-Ichi Usami
Journal:  Hum Genome Var       Date:  2018-08-22

4.  Prevalence and clinical features of hearing loss caused by EYA4 variants.

Authors:  Jun Shinagawa; Hideaki Moteki; Shin-Ya Nishio; Kenji Ohyama; Koshi Otsuki; Satoshi Iwasaki; Shin Masuda; Chie Oshikawa; Yumi Ohta; Yasuhiro Arai; Masahiro Takahashi; Naoko Sakuma; Satoko Abe; Yuika Sakurai; Hirofumi Sakaguchi; Takashi Ishino; Natsumi Uehara; Shin-Ichi Usami
Journal:  Sci Rep       Date:  2020-02-27       Impact factor: 4.379

5.  Genetic background in late-onset sensorineural hearing loss patients.

Authors:  Natsumi Uehara; Takeshi Fujita; Daisuke Yamashita; Jun Yokoi; Sayaka Katsunuma; Akinobu Kakigi; Shin-Ya Nishio; Ken-Ichi Nibu; Shin-Ichi Usami
Journal:  J Hum Genet       Date:  2021-11-26       Impact factor: 3.172

  5 in total

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