Literature DB >> 19235794

Audiologic and temporal bone imaging findings in patients with sensorineural hearing loss and GJB2 mutations.

Kenneth H Lee1, Daniel A Larson, Gordon Shott, Brian Rasmussen, Aliza P Cohen, Corning Benton, Mark Halsted, Daniel Choo, Jareen Meinzen-Derr, John H Greinwald.   

Abstract

OBJECTIVES/HYPOTHESIS: Our objectives were to determine genotype-phenotype correlations in patients with sensorineural hearing loss (SNHL) who undergo testing for GJB2 mutations and to examine the relationship of temporal bone anomalies seen on computed tomography (CT) and GJB2 mutations. STUDY
DESIGN: We conducted a retrospective review of all children diagnosed with SNHL and who underwent GJB2 testing from 1997 to 2006.
RESULTS: Of 840 patients, 146 (17.4%) had mutations. Seventy-six (9.1%) had biallelic GJB2 mutations and 70 (8.3%) had heterozygous mutations. When biallelic mutations were categorized as missense or nonsense mutations, the presence of at least one missense mutation was associated with mild or moderate SNHL. Biallelic nonsense mutations were associated with severe to profound SNHL. Among patients with GJB2 mutations, those with heterozygous mutations (n = 14 [20%]) had a higher rate of asymmetric SNHL loss than those with biallelic mutations (n = 6 [7.9%], P = .03). Those with heterozygous mutations were more likely to experience progression than were those with biallelic mutations, though this difference was only marginally significant (26.5% vs. 12.3%, respectively; P = .06). Patients who were wild type for GJB2 were more likely to have an enlarged vestibular aqueduct (EVA) than were those with biallelic and heterozygous mutations (29% vs. 11.9%, respectively; P = .004). Compared to patients who were wild type, those with biallelic mutations had a significantly lower rate of EVA.
CONCLUSIONS: This is the largest single-institution study of pediatric patients with GJB2 mutations and SNHL. The functional consequences of GJB2 mutations correlated with the degree of hearing loss. Patients with M34T mutations and/or mild SNHL had a low risk of progression. Temporal bone anomalies were uncommon in patients with GJB2 mutations.

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Year:  2009        PMID: 19235794      PMCID: PMC7065710          DOI: 10.1002/lary.20162

Source DB:  PubMed          Journal:  Laryngoscope        ISSN: 0023-852X            Impact factor:   3.325


  17 in total

1.  Connexin 26 mutations in hereditary non-syndromic sensorineural deafness.

Authors:  D P Kelsell; J Dunlop; H P Stevens; N J Lench; J N Liang; G Parry; R F Mueller; I M Leigh
Journal:  Nature       Date:  1997-05-01       Impact factor: 49.962

Review 2.  Newborn hearing screening--a silent revolution.

Authors:  Cynthia C Morton; Walter E Nance
Journal:  N Engl J Med       Date:  2006-05-18       Impact factor: 91.245

3.  Temporal bone imaging in GJB2 deafness.

Authors:  Evan J Propst; Susan Blaser; Tracy L Stockley; Robert V Harrison; Karen A Gordon; Blake C Papsin
Journal:  Laryngoscope       Date:  2006-12       Impact factor: 3.325

4.  The influence of mutations in the SLC26A4 gene on the temporal bone in a population with enlarged vestibular aqueduct.

Authors:  Colm Madden; Mark Halsted; Jareen Meinzen-Derr; Dianna Bardo; Mark Boston; Ellis Arjmand; Carla Nishimura; Tao Yang; Corning Benton; Vijay Das; Richard Smith; Daniel Choo; John Greinwald
Journal:  Arch Otolaryngol Head Neck Surg       Date:  2007-02

5.  GJB2 mutations and degree of hearing loss: a multicenter study.

Authors:  Rikkert L Snoeckx; Patrick L M Huygen; Delphine Feldmann; Sandrine Marlin; Françoise Denoyelle; Jaroslaw Waligora; Malgorzata Mueller-Malesinska; Agneszka Pollak; Rafal Ploski; Alessandra Murgia; Eva Orzan; Pierangela Castorina; Umberto Ambrosetti; Ewa Nowakowska-Szyrwinska; Jerzy Bal; Wojciech Wiszniewski; Andreas R Janecke; Doris Nekahm-Heis; Pavel Seeman; Olga Bendova; Margaret A Kenna; Anna Frangulov; Heidi L Rehm; Mustafa Tekin; Armagan Incesulu; Hans-Henrik M Dahl; Desirée du Sart; Lucy Jenkins; Deirdre Lucas; Maria Bitner-Glindzicz; Karen B Avraham; Zippora Brownstein; Ignacio del Castillo; Felipe Moreno; Nikolaus Blin; Markus Pfister; Istvan Sziklai; Timea Toth; Philip M Kelley; Edward S Cohn; Lionel Van Maldergem; Pascale Hilbert; Anne-Françoise Roux; Michel Mondain; Lies H Hoefsloot; Cor W R J Cremers; Tuija Löppönen; Heikki Löppönen; Agnete Parving; Karen Gronskov; Iris Schrijver; Joseph Roberson; Francesca Gualandi; Alessandro Martini; Geneviéve Lina-Granade; Nathalie Pallares-Ruiz; Céu Correia; Graça Fialho; Kim Cryns; Nele Hilgert; Paul Van de Heyning; Carla J Nishimura; Richard J H Smith; Guy Van Camp
Journal:  Am J Hum Genet       Date:  2005-10-19       Impact factor: 11.025

6.  Carrier rates in the midwestern United States for GJB2 mutations causing inherited deafness.

Authors:  G E Green; D A Scott; J M McDonald; G G Woodworth; V C Sheffield; R J Smith
Journal:  JAMA       Date:  1999-06-16       Impact factor: 56.272

7.  Outcomes of clinical examination and genetic testing of 500 individuals with hearing loss evaluated through a genetics of hearing loss clinic.

Authors:  Dinah Yaeger; Jennifer McCallum; Kathy Lewis; Lisa Soslow; Udayan Shah; William Potsic; Catherine Stolle; Ian D Krantz
Journal:  Am J Med Genet A       Date:  2006-04-15       Impact factor: 2.802

8.  Genotypic and phenotypic correlations of DFNB1-related hearing impairment in the Midwestern United States.

Authors:  Lynne H Y Lim; John K Bradshaw; Yingshi Guo; Valentina Pilipenko; Colm Madden; David Ingala; Mehdi Keddache; Daniel I Choo; Richard Wenstrup; John H Greinwald
Journal:  Arch Otolaryngol Head Neck Surg       Date:  2003-08

9.  M34T and V37I mutations in GJB2 associated hearing impairment: evidence for pathogenicity and reduced penetrance.

Authors:  Agnieszka Pollak; Agata Skórka; Małgorzata Mueller-Malesińska; Grazyna Kostrzewa; Bartłomiej Kisiel; Jarosław Waligóra; Paweł Krajewski; Monika Ołdak; Lech Korniszewski; Henryk Skarzyński; Rafal Ploski
Journal:  Am J Med Genet A       Date:  2007-11-01       Impact factor: 2.802

10.  Connexin-26 mutations in sporadic and inherited sensorineural deafness.

Authors:  X Estivill; P Fortina; S Surrey; R Rabionet; S Melchionda; L D'Agruma; E Mansfield; E Rappaport; N Govea; M Milà; L Zelante; P Gasparini
Journal:  Lancet       Date:  1998-02-07       Impact factor: 79.321

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  6 in total

Review 1.  Diagnostic yield of computed tomography scan for pediatric hearing loss: a systematic review.

Authors:  Jenny X Chen; Bart Kachniarz; Jennifer J Shin
Journal:  Otolaryngol Head Neck Surg       Date:  2014-09-03       Impact factor: 3.497

2.  Temporal bone abnormalities in children with GJB2 mutations.

Authors:  Margaret A Kenna; Heidi L Rehm; Anna Frangulov; Henry A Feldman; Caroline D Robson
Journal:  Laryngoscope       Date:  2011-02-04       Impact factor: 3.325

Review 3.  Cellular and Deafness Mechanisms Underlying Connexin Mutation-Induced Hearing Loss - A Common Hereditary Deafness.

Authors:  Jeffrey C Wingard; Hong-Bo Zhao
Journal:  Front Cell Neurosci       Date:  2015-05-29       Impact factor: 5.505

4.  Functional Testing of SLC26A4 Variants-Clinical and Molecular Analysis of a Cohort with Enlarged Vestibular Aqueduct from Austria.

Authors:  Sebastian Roesch; Emanuele Bernardinelli; Charity Nofziger; Miklós Tóth; Wolfgang Patsch; Gerd Rasp; Markus Paulmichl; Silvia Dossena
Journal:  Int J Mol Sci       Date:  2018-01-10       Impact factor: 5.923

Review 5.  DFNB1 Non-syndromic Hearing Impairment: Diversity of Mutations and Associated Phenotypes.

Authors:  Francisco J Del Castillo; Ignacio Del Castillo
Journal:  Front Mol Neurosci       Date:  2017-12-22       Impact factor: 5.639

6.  Hearing Phenotypes of Patients with Hearing Loss Homozygous for the GJB2 c.235delc Mutation.

Authors:  Chang Guo; Sha-Sha Huang; Yong-Yi Yuan; Ying Zhou; Ning Wang; Dong-Yang Kang; Su-Yan Yang; Xin Zhang; Xue Gao; Pu Dai
Journal:  Neural Plast       Date:  2020-08-01       Impact factor: 3.599

  6 in total

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