Literature DB >> 17365059

The changing face of Usher syndrome: clinical implications.

Mazal Cohen1, Maria Bitner-Glindzicz, Linda Luxon.   

Abstract

Usher syndrome is both genetically and phenotypically heterogeneous. Traditionally, the condition has been classified into three clinical types, differentiated by the severity and progression of the hearing impairment and by the presence or absence of vestibular symptoms. Recent advances in molecular genetics have enabled researchers to study the phenotypic expression in confirmed molecular groups of Usher. In response to the expansion of clinical and genetic information on Usher, we report an up to date review of the different clinical forms of Usher in known molecular groups and use the emerging evidence to appraise the diagnostic utility of the traditional classification of Usher. Our findings undermine the traditional view that the clinical types of Usher have distinct genetic causes. The pleiotropic effects of some of the major causes of Usher lead to considerable overlap between the different clinical types, with very little evidence for phenotypic-genotypic correlations. The novel synthesis emerging from this review suggests more productive approaches to the diagnosis of Usher in hearing-impaired children which would provide more accurate prognostic information to families.

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Year:  2007        PMID: 17365059     DOI: 10.1080/14992020600975279

Source DB:  PubMed          Journal:  Int J Audiol        ISSN: 1499-2027            Impact factor:   2.117


  24 in total

1.  Novel and recurrent CIB2 variants, associated with nonsyndromic deafness, do not affect calcium buffering and localization in hair cells.

Authors:  Celia Zazo Seco; Arnaud P Giese; Sobia Shafique; Margit Schraders; Anne M M Oonk; Mike Grossheim; Jaap Oostrik; Tim Strom; Rashmi Hegde; Erwin van Wijk; Gregory I Frolenkov; Maleeha Azam; Helger G Yntema; Rolien H Free; Saima Riazuddin; Joke B G M Verheij; Ronald J Admiraal; Raheel Qamar; Zubair M Ahmed; Hannie Kremer
Journal:  Eur J Hum Genet       Date:  2015-07-15       Impact factor: 4.246

2.  PDZD7 is a modifier of retinal disease and a contributor to digenic Usher syndrome.

Authors:  Inga Ebermann; Jennifer B Phillips; Max C Liebau; Robert K Koenekoop; Bernhard Schermer; Irma Lopez; Ellen Schäfer; Anne-Francoise Roux; Claudia Dafinger; Antje Bernd; Eberhart Zrenner; Mireille Claustres; Bernardo Blanco; Gudrun Nürnberg; Peter Nürnberg; Rebecca Ruland; Monte Westerfield; Thomas Benzing; Hanno J Bolz
Journal:  J Clin Invest       Date:  2010-05-03       Impact factor: 14.808

3.  Genetic analysis of 10 pedigrees with inherited retinal degeneration by exome sequencing and phenotype-genotype association.

Authors:  Pooja Biswas; Jacque L Duncan; Bruno Maranhao; Igor Kozak; Kari Branham; Luis Gabriel; Jonathan H Lin; Giulio Barteselli; Mili Navani; John Suk; Michelle Parke; Catherine Schlechter; Richard G Weleber; John R Heckenlively; Gislin Dagnelie; Pauline Lee; S Amer Riazuddin; Radha Ayyagari
Journal:  Physiol Genomics       Date:  2017-01-27       Impact factor: 3.107

4.  Loss of Ca(v)1.3 (CACNA1D) function in a human channelopathy with bradycardia and congenital deafness.

Authors:  Shahid M Baig; Alexandra Koschak; Andreas Lieb; Mathias Gebhart; Claudia Dafinger; Gudrun Nürnberg; Amjad Ali; Ilyas Ahmad; Martina J Sinnegger-Brauns; Niels Brandt; Jutta Engel; Matteo E Mangoni; Muhammad Farooq; Habib U Khan; Peter Nürnberg; Jörg Striessnig; Hanno J Bolz
Journal:  Nat Neurosci       Date:  2010-12-05       Impact factor: 24.884

5.  An USH2A founder mutation is the major cause of Usher syndrome type 2 in Canadians of French origin and confirms common roots of Quebecois and Acadians.

Authors:  Inga Ebermann; Robert K Koenekoop; Irma Lopez; Lara Bou-Khzam; Renée Pigeon; Hanno J Bolz
Journal:  Eur J Hum Genet       Date:  2008-07-30       Impact factor: 4.246

6.  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

7.  A large deletion in GPR98 causes type IIC Usher syndrome in male and female members of an Iranian family.

Authors:  N Hilgert; K Kahrizi; N Dieltjens; N Bazazzadegan; H Najmabadi; R J H Smith; G Van Camp
Journal:  J Med Genet       Date:  2009-04       Impact factor: 6.318

8.  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

9.  The shaker-1 mouse myosin VIIa deafness mutation results in a severely reduced rate of the ATP hydrolysis step.

Authors:  Ailian Xiong; Jessica Haithcock; Yingying Liu; Lauren Eusner; Matthew McConnell; Howard D White; Betty Belknap; Eva Forgacs
Journal:  J Biol Chem       Date:  2017-11-22       Impact factor: 5.157

10.  Disease-causing mutations in the CLRN1 gene alter normal CLRN1 protein trafficking to the plasma membrane.

Authors:  Juha Isosomppi; Hanna Västinsalo; Scott F Geller; Elise Heon; John G Flannery; Eeva-Marja Sankila
Journal:  Mol Vis       Date:  2009-09-08       Impact factor: 2.367

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