Literature DB >> 20621367

Screening of SLC26A4, FOXI1 and KCNJ10 genes in unilateral hearing impairment with ipsilateral enlarged vestibular aqueduct.

Laurence Jonard1, Magali Niasme-Grare, Crystel Bonnet, Delphine Feldmann, Isabelle Rouillon, Natalie Loundon, Catherine Calais, Hélène Catros, Albert David, Hélène Dollfus, Valérie Drouin-Garraud, Françoise Duriez, Marie Madeleine Eliot, Florence Fellmann, Christine Francannet, Brigitte Gilbert-Dussardier, Catherine Gohler, Cyril Goizet, Hubert Journel, Thierry Mom, Marie-Françoise Thuillier-Obstoy, Remy Couderc, Eréa Noël Garabédian, Françoise Denoyelle, Sandrine Marlin.   

Abstract

OBJECTIVE: To investigate the implication of SLC26A4, FOXI and KCNJ10 genes in unilateral hearing impairment associated with ipsilateral inner ear malformation (Enlargement of the vestibular aqueduct and/or Mondini dysplasia).
METHODS: We have gathered 25 patients presenting unilateral hearing impairment and ipsilateral enlarged vestibular aqueduct. For each of the patients, we have analyzed SLC26A4, FOXI1 and KCNJ10 genes sequences.
RESULTS: The analysis of SLC26A4 revealed only eight heterozygous SLC26A4 sequence variants, three of them being novel (p.Met147Ile, p.Asn538Asn and p.Leu627Arg). None of the patients carried a second mutation on the other allele. Moreover, the SLC26A4 locus was excluded by segregation analysis in two families. No mutations were present in FOXI1 and KCNJ10 genes.
CONCLUSIONS: Together, these data suggest that SLC26A4, FOXI1 and KCNJ10 are not major determinants in unilateral deafness and enlarged vestibular aqueduct compared with their implication in Pendred syndrome and non-syndromic bilateral enlarged vestibular aqueduct. Copyright 2010 Elsevier Ireland Ltd. All rights reserved.

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Year:  2010        PMID: 20621367     DOI: 10.1016/j.ijporl.2010.06.002

Source DB:  PubMed          Journal:  Int J Pediatr Otorhinolaryngol        ISSN: 0165-5876            Impact factor:   1.675


  17 in total

1.  Atypical patterns of segregation of familial enlargement of the vestibular aqueduct.

Authors:  Julie A Muskett; Parna Chattaraj; John F Heneghan; Fabian R Reimold; Boris E Shmukler; Carmen C Brewer; Kelly A King; Christopher K Zalewski; Thomas H Shawker; John A Butman; Margaret A Kenna; Wade W Chien; Seth L Alper; Andrew J Griffith
Journal:  Laryngoscope       Date:  2015-10-20       Impact factor: 3.325

2.  A common SLC26A4-linked haplotype underlying non-syndromic hearing loss with enlargement of the vestibular aqueduct.

Authors:  Parna Chattaraj; Tina Munjal; Keiji Honda; Nanna D Rendtorff; Jessica S Ratay; Julie A Muskett; Davide S Risso; Isabelle Roux; E Michael Gertz; Alejandro A Schäffer; Thomas B Friedman; Robert J Morell; Lisbeth Tranebjærg; Andrew J Griffith
Journal:  J Med Genet       Date:  2017-08-05       Impact factor: 6.318

Review 3.  SLC26A4 genotypes and phenotypes associated with enlargement of the vestibular aqueduct.

Authors:  Taku Ito; Byung Yoon Choi; Kelly A King; Christopher K Zalewski; Julie Muskett; Parna Chattaraj; Thomas Shawker; James C Reynolds; John A Butman; Carmen C Brewer; Philine Wangemann; Seth L Alper; Andrew J Griffith
Journal:  Cell Physiol Biochem       Date:  2011-11-18

Review 4.  Hearing loss associated with enlargement of the vestibular aqueduct: mechanistic insights from clinical phenotypes, genotypes, and mouse models.

Authors:  Andrew J Griffith; Philine Wangemann
Journal:  Hear Res       Date:  2011-06-06       Impact factor: 3.208

5.  SLC26A4 mutation testing for hearing loss associated with enlargement of the vestibular aqueduct.

Authors:  Taku Ito; Julie Muskett; Parna Chattaraj; Byung Yoon Choi; Kyu Yup Lee; Christopher K Zalewski; Kelly A King; Xiangming Li; Philine Wangemann; Thomas Shawker; Carmen C Brewer; Seth L Alper; Andrew J Griffith
Journal:  World J Otorhinolaryngol       Date:  2013-05-28

Review 6.  The role of an inwardly rectifying K(+) channel (Kir4.1) in the inner ear and hearing loss.

Authors:  J Chen; H-B Zhao
Journal:  Neuroscience       Date:  2014-01-28       Impact factor: 3.590

7.  Assessment of the Clinical Benefit of Imaging in Children With Unilateral Sensorineural Hearing Loss: A Systematic Review and Meta-analysis.

Authors:  Fabienne G Ropers; Eveline N B Pham; Sarina G Kant; Liselotte J C Rotteveel; Edmond H H M Rings; Berit M Verbist; Olaf M Dekkers
Journal:  JAMA Otolaryngol Head Neck Surg       Date:  2019-05-01       Impact factor: 6.223

Review 8.  Development and Patterning of the Cochlea: From Convergent Extension to Planar Polarity.

Authors:  Mireille Montcouquiol; Matthew W Kelley
Journal:  Cold Spring Harb Perspect Med       Date:  2020-01-02       Impact factor: 6.915

Review 9.  Genetic architecture and phenotypic landscape of SLC26A4-related hearing loss.

Authors:  Keiji Honda; Andrew J Griffith
Journal:  Hum Genet       Date:  2021-08-03       Impact factor: 4.132

10.  Enlarged vestibular aqueduct and Mondini Malformation: audiological, clinical, radiologic and genetic features.

Authors:  F Forli; F Lazzerini; G Auletta; L Bruschini; S Berrettini
Journal:  Eur Arch Otorhinolaryngol       Date:  2020-09-10       Impact factor: 2.503

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