The DFNA10 phenotype

被引:11
作者
De Leenheer, EMR
Huygen, PLM
Wayne, S
Smith, RJH
Cremers, WRJ
机构
[1] Univ Nijmegen Hosp, Dept Otorhinolaryngol, NL-6500 HB Nijmegen, Netherlands
[2] Univ Iowa, Dept Otolaryngol Head & Neck Surg, Mol Otolaryngol Res Labs, Iowa City, IA USA
关键词
autosomal dominant nonsyndromic; hearing loss; DFNA10; speech discrimination;
D O I
10.1177/000348940111000910
中图分类号
R76 [耳鼻咽喉科学];
学科分类号
100213 ;
摘要
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 DFNA16 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.
引用
收藏
页码:861 / 866
页数:6
相关论文
共 6 条
[1]  
International Standards Organization (ISO), 1984, 7029 ISO
[2]  
Motulsky H., 1995, INTUITIVE BIOSTATIST
[3]   Gene for autosomal dominant late-onset progressive non-syndromic hearing loss, DFNA10, maps to chromosome 6 [J].
ONeill, ME ;
Marietta, J ;
Nishimura, D ;
Wayne, S ;
VanCamp, G ;
VanLaer, L ;
Negrini, C ;
Wilcox, ER ;
Chen, A ;
Fukushima, K ;
Ni, L ;
Sheffield, VC ;
Smith, RJH .
HUMAN MOLECULAR GENETICS, 1996, 5 (06) :853-856
[4]  
VANCAMP G, 2001, HEREDITARY HEARING L
[5]   Mutations in the transcriptional activator EYA4 cause late-onset deafness at the DFNA10 locus [J].
Wayne, S ;
Robertson, NG ;
DeClau, F ;
Chen, N ;
Verhoeven, K ;
Prasad, S ;
Tranebjärg, L ;
Morton, CC ;
Ryan, AF ;
Van Camp, G ;
Smith, RJH .
HUMAN MOLECULAR GENETICS, 2001, 10 (03) :195-200
[6]  
1996, EUR WORK GROUP GENET