Literature DB >> 16830115

Enlarged vestibular aqueduct: Looking for genotypic-phenotypic correlations.

José Angel González-García1, Andrés Ibáñez, Rafael Ramírez-Camacho, Antonio Rodríguez, José Ramón García-Berrocal, Almudena Trinidad.   

Abstract

The aim of this work is to provide a guide for clinical and genetic diagnosis and classification of the enlarged vestibular aqueduct syndrome based on a review of the literature and computerized databases with the words large and enlarged vestibular aqueduct. No more than 40 articles described association between the EVA phenotype and a known genetic alteration. Pendred's syndrome, distal renal tubular acidosis, waardenburg's syndrome, X-linked congenital mixed deafness, branchio-oto-renal syndrome, and oto-facio-cervical syndrome can express their genotypic alteration as enlarged vestibular aqueduct syndrome. We also found articles reporting familiar cases of enlarged vestibular aqueduct with no identified mutations in studied genes.

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Year:  2006        PMID: 16830115     DOI: 10.1007/s00405-006-0095-x

Source DB:  PubMed          Journal:  Eur Arch Otorhinolaryngol        ISSN: 0937-4477            Impact factor:   2.503


  24 in total

1.  The gene for X-linked progressive mixed deafness with perilymphatic gusher during stapes surgery (DFN3) is linked to PGK.

Authors:  H G Brunner; A van Bennekom; E M Lambermon; T L Oei; W R Cremers; B Wieringa; H H Ropers
Journal:  Hum Genet       Date:  1988-12       Impact factor: 4.132

2.  Immune response and immunopathology of the inner ear: an update.

Authors:  J R García Berrocal; R Ramírez-Camacho
Journal:  J Laryngol Otol       Date:  2000-02       Impact factor: 1.469

3.  The large vestibular aqueduct syndrome.

Authors:  G E Valvassori; J D Clemis
Journal:  Laryngoscope       Date:  1978-05       Impact factor: 3.325

4.  Non-syndromic hearing loss associated with enlarged vestibular aqueduct is caused by PDS mutations.

Authors:  S Usami; S Abe; M D Weston; H Shinkawa; G Van Camp; W J Kimberling
Journal:  Hum Genet       Date:  1999-02       Impact factor: 4.132

5.  The presence of a widened vestibular aqueduct and progressive sensorineural hearing loss in the branchio-oto-renal syndrome. A family study.

Authors:  C Stinckens; L Standaert; J W Casselman; P L Huygen; S Kumar; J Van de Wallen; C W Cremers
Journal:  Int J Pediatr Otorhinolaryngol       Date:  2001-07-02       Impact factor: 1.675

6.  Pendred syndrome is caused by mutations in a putative sulphate transporter gene (PDS).

Authors:  L A Everett; B Glaser; J C Beck; J R Idol; A Buchs; M Heyman; F Adawi; E Hazani; E Nassir; A D Baxevanis; V C Sheffield; E D Green
Journal:  Nat Genet       Date:  1997-12       Impact factor: 38.330

7.  Audiometric findings in children with a large vestibular aqueduct.

Authors:  Ellis M Arjmand; Audra Webber
Journal:  Arch Otolaryngol Head Neck Surg       Date:  2004-10

8.  Waardenburg syndrome type 2 caused by mutations in the human microphthalmia (MITF) gene.

Authors:  M Tassabehji; V E Newton; A P Read
Journal:  Nat Genet       Date:  1994-11       Impact factor: 38.330

9.  Computed tomographic diagnosis of X-linked congenital mixed deafness, fixation of the stapedial footplate, and perilymphatic gusher.

Authors:  J M Talbot; D F Wilson
Journal:  Am J Otol       Date:  1994-03

10.  Waardenburg's syndrome patients have mutations in the human homologue of the Pax-3 paired box gene.

Authors:  M Tassabehji; A P Read; V E Newton; R Harris; R Balling; P Gruss; T Strachan
Journal:  Nature       Date:  1992-02-13       Impact factor: 49.962

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  4 in total

Review 1.  Imaging of congenital anomalies and acquired lesions of the inner ear.

Authors:  Gabriele A Krombach; Dagmar Honnef; Martin Westhofen; Ercole Di Martino; Rolf W Günther
Journal:  Eur Radiol       Date:  2007-10-10       Impact factor: 5.315

Review 2.  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

3.  Inner ear abnormalities in four patients with dRTA and SNHL: clinical and genetic heterogeneity.

Authors:  Elena Andreucci; Benedetta Bianchi; Ilaria Carboni; Giancarlo Lavoratti; Marzia Mortilla; Claudio Fonda; Minna Bigozzi; Maurizio Genuardi; Sabrina Giglio; Ivana Pela
Journal:  Pediatr Nephrol       Date:  2009-07-29       Impact factor: 3.714

4.  Cerebrospinal Fluid Leak in Cochlear Implantation: Enlarged Cochlear versus Enlarged Vestibular Aqueduct (Common Cavity Excluded).

Authors:  Giovanni Bianchin; Valeria Polizzi; Patrizia Formigoni; Carmela Russo; Lorenzo Tribi
Journal:  Int J Otolaryngol       Date:  2016-10-26
  4 in total

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