Literature DB >> 2817677

Progressive hearing loss in Usher's syndrome.

S Karjalainen1, L Pakarinen, M Teräsvirta, H Kääriäinen, E Vartiainen.   

Abstract

In 18 patients with Usher's syndrome, progressive hearing loss was verified audiologically in eight cases. Despite poor auditory threshold values and low speech discrimination scores, there was only one patient who could not communicate with speech. The possibility of hearing impairment being mainly progressive in Usher's syndrome is discussed.

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Mesh：

Year:  1989        PMID： 2817677     DOI： 10.1177/000348948909801106

Source DB:  PubMed          Journal:  Ann Otol Rhinol Laryngol        ISSN： 0003-4894            Impact factor:   1.547


  8 in total

Review 1.  The Finnish Disease Heritage III: the individual diseases.

Authors:  Reijo Norio
Journal:  Hum Genet       Date:  2003-03-08       Impact factor: 4.132

2.  Genetic heterogeneity of Usher syndrome type II in a Dutch population.

Authors:  S Pieke-Dahl; A van Aarem; A Dobin; C W Cremers; W J Kimberling
Journal:  J Med Genet       Date:  1996-09       Impact factor: 6.318

3.  Genetic heterogeneity of Usher syndrome type II: localisation to chromosome 5q.

Authors:  S Pieke-Dahl; C G Möller; P M Kelley; L M Astuto; C W Cremers; M B Gorin; W J Kimberling
Journal:  J Med Genet       Date:  2000-04       Impact factor: 6.318

4.  Retinitis pigmentosa and progressive sensorineural hearing loss caused by a C12258A mutation in the mitochondrial MTTS2 gene.

Authors:  F C Mansergh; S Millington-Ward; A Kennan; A S Kiang; M Humphries; G J Farrar; P Humphries; P F Kenna
Journal:  Am J Hum Genet       Date:  1999-04       Impact factor: 11.025

5.  Mutation analysis in the long isoform of USH2A in American patients with Usher Syndrome type II.

Authors:  Denise Yan; Xiaomei Ouyang; D Michael Patterson; Li Lin Du; Samuel G Jacobson; Xue-Zhong Liu
Journal:  J Hum Genet       Date:  2009-10-30       Impact factor: 3.172

6.  Cone structure in patients with usher syndrome type III and mutations in the Clarin 1 gene.

Authors:  Kavitha Ratnam; Hanna Västinsalo; Austin Roorda; Eeva-Marja K Sankila; Jacque L Duncan
Journal:  JAMA Ophthalmol       Date:  2013-01       Impact factor: 7.389

7.  Linkage analysis in Usher syndrome type I (USH1) families from Spain.

Authors:  C Espinós; C Nájera; J M Millán; C Ayuso; M Baiget; H Pérez-Garrigues; O Rodrigo; C Vilela; M Beneyto
Journal:  J Med Genet       Date:  1998-05       Impact factor: 6.318

8.  Gene mapping of Usher syndrome type IIa: localization of the gene to a 2.1-cM segment on chromosome 1q41.

Authors:  W J Kimberling; M D Weston; C Möller; A van Aarem; C W Cremers; J Sumegi; P S Ing; C Connolly; A Martini; M Milani
Journal:  Am J Hum Genet       Date:  1995-01       Impact factor: 11.025
  8 in total

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