Literature DB >> 16151338

Vestibular deterioration precedes hearing deterioration in the P51S COCH mutation (DFNA9): an analysis in 74 mutation carriers.

Anne M L C Bischoff1, Patrick L M Huygen, Martijn H Kemperman, Ronald J E Pennings, Steven J H Bom, Wim I M Verhagen, Ronald J C Admiraal, Hannie Kremer, Cor W R J Cremers.   

Abstract

OBJECTIVES: To analyze cochleovestibular impairment features in P51S COCH mutation carriers (n = 22) in a new, large Dutch family and to compare the results to those obtained in previously identified similar mutation carriers (n = 52). To evaluate age-related features between progressive hearing and vestibular impairment of all mutation carriers (n = 74). STUDY
DESIGN: Family study.
METHODS: Regression analysis was performed in relation to age to outline the development of hearing thresholds, speech recognition scores, and vestibulo-ocular reflex time constant as the key vestibular response parameter.
RESULTS: Pure tone thresholds, phoneme recognition scores, and vestibular responses of the mutation carriers in the new family were essentially similar to those previously established in all other mutation carriers. Hearing started to deteriorate in all mutation carriers from 43 years of age onwards, whereas deterioration of vestibular function started from age 34.
CONCLUSION: Vestibular impairment starts earlier, progresses more rapidly, and, eventually, is more complete than hearing impairment in P51S COCH mutation carriers.

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Year:  2005        PMID: 16151338     DOI: 10.1097/01.mao.0000185048.84641.e3

Source DB:  PubMed          Journal:  Otol Neurotol        ISSN: 1531-7129            Impact factor:   2.311


  14 in total

1.  Hearing and vestibular deficits in the Coch(-/-) null mouse model: comparison to the Coch(G88E/G88E) mouse and to DFNA9 hearing and balance disorder.

Authors:  Sherri M Jones; Nahid G Robertson; Shelly Given; Anne B S Giersch; M Charles Liberman; Cynthia C Morton
Journal:  Hear Res       Date:  2010-11-10       Impact factor: 3.208

2.  Extralabyrinthine manifestations of DFNA9.

Authors:  Andrew A McCall; Fred H Linthicum; Jennifer T O'Malley; Joe C Adams; Saumil N Merchant; Marc K Bassim; Robert Gellibolian; Jose N Fayad
Journal:  J Assoc Res Otolaryngol       Date:  2010-11-04

3.  Bi-allelic inactivating variants in the COCH gene cause autosomal recessive prelingual hearing impairment.

Authors:  Sebastien P F JanssensdeVarebeke; Guy Van Camp; Nils Peeters; Ellen Elinck; Josine Widdershoven; Tony Cox; Kristof Deben; Katrien Ketelslagers; Tom Crins; Wim Wuyts
Journal:  Eur J Hum Genet       Date:  2018-02-15       Impact factor: 4.246

4.  Bayesian quantification of sensory reweighting in a familial bilateral vestibular disorder (DFNA9).

Authors:  Bart B G T Alberts; Luc P J Selen; Wim I M Verhagen; Ronald J E Pennings; W Pieter Medendorp
Journal:  J Neurophysiol       Date:  2017-12-13       Impact factor: 2.714

5.  A targeted Coch missense mutation: a knock-in mouse model for DFNA9 late-onset hearing loss and vestibular dysfunction.

Authors:  Nahid G Robertson; Sherri M Jones; Theru A Sivakumaran; Anne B S Giersch; Sara A Jurado; Linda M Call; Constance E Miller; Stéphane F Maison; M Charles Liberman; Cynthia C Morton
Journal:  Hum Mol Genet       Date:  2008-08-12       Impact factor: 6.150

6.  Mutation in the COCH gene is associated with superior semicircular canal dehiscence.

Authors:  Michael S Hildebrand; Dylan Tack; Adam Deluca; In Ae Hur; Jana M Van Rybroek; Sarah J McMordie; Ann Muilenburg; David P Hoskinson; Guy Van Camp; Myles L Pensak; Ian S Storper; Patrick L M Huygen; Thomas L Casavant; Richard J H Smith
Journal:  Am J Med Genet A       Date:  2009-02       Impact factor: 2.802

7.  Sensory substitution in bilateral vestibular a-reflexic patients.

Authors:  Bart B G T Alberts; Luc P J Selen; Wim I M Verhagen; W Pieter Medendorp
Journal:  Physiol Rep       Date:  2015-05

8.  Massively Parallel Sequencing of a Chinese Family with DFNA9 Identified a Novel Missense Mutation in the LCCL Domain of COCH.

Authors:  Xiaodong Gu; Wenling Su; Mingliang Tang; Luo Guo; Liping Zhao; Huawei Li
Journal:  Neural Plast       Date:  2016-12-27       Impact factor: 3.599

9.  Identification of a rare COCH mutation by whole-exome sequencing : Implications for personalized therapeutic rehabilitation in an Austrian family with non-syndromic autosomal dominant late-onset hearing loss.

Authors:  Thomas Parzefall; Alexandra Frohne; Martin Koenighofer; Andreas Kirchnawy; Berthold Streubel; Christian Schoefer; Wolfgang Gstoettner; Klemens Frei; Trevor Lucas
Journal:  Wien Klin Wochenschr       Date:  2017-07-21       Impact factor: 1.704

10.  Does Otovestibular Loss in the Autosomal Dominant Disorder DFNA9 Have an Impact of on Cognition? A Systematic Review.

Authors:  Jonas De Belder; Stijn Matthysen; Annes J Claes; Griet Mertens; Paul Van de Heyning; Vincent Van Rompaey
Journal:  Front Neurosci       Date:  2018-01-09       Impact factor: 4.677

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