Literature DB >> 21895633

Audiological findings in 100 USH2 patients.

C Abadie1, C Blanchet, D Baux, L Larrieu, T Besnard, P Ravel, R Biboulet, C Hamel, S Malcolm, M Mondain, M Claustres, A-F Roux.   

Abstract

Bilateral sensorineural hearing loss (HL), classically described as mild to severe with a typically down-sloping audiometric configuration, is the earliest symptom occurring in Usher syndrome type II (USH2). Audiological findings were analyzed in a total of 100 USH2 patients (92 families) divided into three groups according to the gene involved: 88 USH2A, 10 GPR98 and 2 DFNB31 patients. A fine analysis of audiograms was performed (pure tone average, degree of severity, configuration). The median age of HL diagnosis was 5 years (range 8 months-31 years) although the median age at USH2 diagnosis was 34.5 (range 8-76). Moderate HL was predominant (76%) and a gently down-sloping configuration characterized most audiograms (66%). No statistically significant difference was found between USH2A and GPR98 patients but a tendency was clearly noted for more GPR98 patients to present with severe hearing loss. It is not possible to predict the mutated gene from audiograms.
© 2011 John Wiley & Sons A/S.

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Year:  2011        PMID: 21895633     DOI: 10.1111/j.1399-0004.2011.01772.x

Source DB:  PubMed          Journal:  Clin Genet        ISSN: 0009-9163            Impact factor:   4.438


  14 in total

1.  Novel compound heterozygous mutations in the GPR98 (USH2C) gene identified by whole exome sequencing in a Moroccan deaf family.

Authors:  Amale Bousfiha; Amina Bakhchane; Hicham Charoute; Mustapha Detsouli; Hassan Rouba; Majida Charif; Guy Lenaers; Abdelhamid Barakat
Journal:  Mol Biol Rep       Date:  2017-09-26       Impact factor: 2.316

2.  USH2 caused by GPR98 mutation diagnosed by massively parallel sequencing in advance of the occurrence of visual symptoms.

Authors:  Hideaki Moteki; Hidekane Yoshimura; Hela Azaiez; Kevin T Booth; A Eliot Shearer; Christina M Sloan; Diana L Kolbe; Toshinori Murata; Richard J H Smith; Shin-Ichi Usami
Journal:  Ann Otol Rhinol Laryngol       Date:  2015-03-05       Impact factor: 1.547

3.  Individual USH2 proteins make distinct contributions to the ankle link complex during development of the mouse cochlear stereociliary bundle.

Authors:  Junhuang Zou; Pranav D Mathur; Tihua Zheng; Yong Wang; Ali Almishaal; Albert H Park; Jun Yang
Journal:  Hum Mol Genet       Date:  2015-09-23       Impact factor: 6.150

4.  Targeted next generation sequencing in Italian patients with Usher syndrome: phenotype-genotype correlations.

Authors:  Chiara M Eandi; Laura Dallorto; Roberta Spinetta; Maria Pia Micieli; Mario Vanzetti; Alessandro Mariottini; Ilaria Passerini; Francesca Torricelli; Camilla Alovisi; Cristiana Marchese
Journal:  Sci Rep       Date:  2017-11-15       Impact factor: 4.379

5.  Novel Usher syndrome pathogenic variants identified in cases with hearing and vision loss.

Authors:  Justin A Pater; Jane Green; Darren D O'Rielly; Anne Griffin; Jessica Squires; Taylor Burt; Sara Fernandez; Bridget Fernandez; Jim Houston; Jiayi Zhou; Nicole M Roslin; Terry-Lynn Young
Journal:  BMC Med Genet       Date:  2019-05-02       Impact factor: 2.103

Review 6.  Genetics, pathogenesis and therapeutic developments for Usher syndrome type 2.

Authors:  M Stemerdink; B García-Bohórquez; R Schellens; G Garcia-Garcia; E Van Wijk; J M Millan
Journal:  Hum Genet       Date:  2021-07-30       Impact factor: 4.132

7.  The contribution of GPR98 and DFNB31 genes to a Spanish Usher syndrome type 2 cohort.

Authors:  Gema García-García; Thomas Besnard; David Baux; Christel Vaché; Elena Aller; Sue Malcolm; Mireille Claustres; Jose M Millan; Anne-Françoise Roux
Journal:  Mol Vis       Date:  2013-02-13       Impact factor: 2.367

8.  Auditory and olfactory findings in patients with USH2A-related retinal degeneration-Findings at baseline from the rate of progression in USH2A-related retinal degeneration natural history study (RUSH2A).

Authors:  Alessandro Iannaccone; Carmen C Brewer; Peiyao Cheng; Jacque L Duncan; Maureen G Maguire; Isabelle Audo; Allison R Ayala; Paul S Bernstein; Gavin M Bidelman; Janet K Cheetham; Richard L Doty; Todd A Durham; Robert B Hufnagel; Mark H Myers; Katarina Stingl; Wadih M Zein
Journal:  Am J Med Genet A       Date:  2021-07-30       Impact factor: 2.578

9.  NGS-based Molecular diagnosis of 105 eyeGENE(®) probands with Retinitis Pigmentosa.

Authors:  Zhongqi Ge; Kristen Bowles; Kerry Goetz; Hendrik P N Scholl; Feng Wang; Xinjing Wang; Shan Xu; Keqing Wang; Hui Wang; Rui Chen
Journal:  Sci Rep       Date:  2015-12-15       Impact factor: 4.379

10.  Severe or Profound Sensorineural Hearing Loss Caused by Novel USH2A Variants in Korea: Potential Genotype-Phenotype Correlation.

Authors:  Sang-Yeon Lee; Kwangsic Joo; Jayoung Oh; Jin Hee Han; Hye-Rim Park; Seungmin Lee; Doo-Yi Oh; Se Joon Woo; Byung Yoon Choi
Journal:  Clin Exp Otorhinolaryngol       Date:  2019-11-02       Impact factor: 3.372

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