Literature DB >> 8203808

Nonsyndromic hearing loss: an analysis of audiograms.

X Liu1, L Xu.   

Abstract

We examined features of the audiograms of 136 individuals, from 28 families, affected by nonsyndromic genetic hearing loss. There were 83 (12 families) with autosomal dominant (AD) loss, 50 (15 families) with autosomal recessive (AR) loss, and 3 (1 family) with X-linked recessive loss. The main audiogram shapes found were sloping (50.3%), residual (26.5%), and flat (21.0%). Specific shapes (ascending and U-shaped) only occurred in 3.7% of AD cases. Audiogram shapes were found to be significantly different between AD and AR families, and showed intrafamilial and interfamilial variability. In the AR group, the main shapes were residual and sharply sloping, and in the AD group, sharply sloping, flat, and gently sloping. There was a significant difference in the degree of hearing loss between AD and AR types, with AD being milder than AR. It has been shown that there is more marked intrafamilial variation in the degree of hearing loss in AD families than in AR ones. The results suggest that the audiograms of nonsyndromic hearing loss are usually nonspecific and that counseling of family members would be better based on the specific family's condition rather than on group information.

Entities:  

Mesh:

Year:  1994        PMID: 8203808     DOI: 10.1177/000348949410300602

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


  13 in total

1.  A novel locus for autosomal dominant non-syndromic deafness, DFNA53, maps to chromosome 14q11.2-q12.

Authors:  D Yan; X Ke; S H Blanton; X M Ouyang; A Pandya; L L Du; W E Nance; X Z Liu
Journal:  J Med Genet       Date:  2005-06-15       Impact factor: 6.318

2.  Sensorineural hearing loss in patients with chronic progressive external ophthalmoplegia or Kearns-Sayre syndrome.

Authors:  C Kornblum; R Broicher; E Walther; S Herberhold; T Klockgether; C Herberhold; R Schröder
Journal:  J Neurol       Date:  2005-04-15       Impact factor: 4.849

Review 3.  Diagnostic and therapeutic applications of genomic medicine in progressive, late-onset, nonsyndromic sensorineural hearing loss.

Authors:  Joaquin E Jimenez; Aida Nourbakhsh; Brett Colbert; Rahul Mittal; Denise Yan; Carlos L Green; Eric Nisenbaum; George Liu; Nicole Bencie; Jason Rudman; Susan H Blanton; Xue Zhong Liu
Journal:  Gene       Date:  2020-04-15       Impact factor: 3.688

4.  Audiological and genetic features of the mtDNA mutations.

Authors:  X Z Liu; S Angeli; X M Ouyang; W Liu; X M Ke; Y H Liu; S X Liu; L L Du; X W Deng; H Yuan; D Yan
Journal:  Acta Otolaryngol       Date:  2008-07       Impact factor: 1.494

Review 5.  Genetics of hearing and deafness.

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Journal:  Anat Rec (Hoboken)       Date:  2012-10-08       Impact factor: 2.064

6.  Targeted massive parallel sequencing: the effective detection of novel causative mutations associated with hearing loss in small families.

Authors:  Jeong-In Baek; Se-Kyung Oh; Dong-Bin Kim; Soo-Young Choi; Un-Kyung Kim; Kyu-Yup Lee; Sang-Heun Lee
Journal:  Orphanet J Rare Dis       Date:  2012-09-03       Impact factor: 4.123

7.  Modifiers of hearing impairment in humans and mice.

Authors:  Denise Yan; Xue-Zhong Liu
Journal:  Curr Genomics       Date:  2010-06       Impact factor: 2.236

8.  Evaluation of the contribution of the EYA4 and GRHL2 genes in Korean patients with autosomal dominant non-syndromic hearing loss.

Authors:  Ye-Ri Kim; Min-A Kim; Borum Sagong; Seung-Hyun Bae; Hyo-Jeong Lee; Hyung-Jong Kim; Jae Young Choi; Kyu-Yup Lee; Un-Kyung Kim
Journal:  PLoS One       Date:  2015-03-17       Impact factor: 3.240

Review 9.  The Genetics of Deafness in Domestic Animals.

Authors:  George M Strain
Journal:  Front Vet Sci       Date:  2015-09-08

10.  Biomarkers of Presbycusis and Tinnitus in a Portuguese Older Population.

Authors:  Haúla F Haider; Marisa Flook; Mariana Aparicio; Diogo Ribeiro; Marilia Antunes; Agnieszka J Szczepek; Derek J Hoare; Graça Fialho; João C Paço; Helena Caria
Journal:  Front Aging Neurosci       Date:  2017-11-01       Impact factor: 5.750

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