Literature DB >> 21358186

Usher syndrome: hearing loss with vision loss.

Thomas B Friedman, Julie M Schultz, Zubair M Ahmed, Ekaterini T Tsilou, Carmen C Brewer.   

Abstract

Usher syndrome (USH) is a clinically heterogeneous condition characterized by sensorineural hearing loss, progressive retinal degeneration, and vestibular dysfunction. A minimum test battery is described as well as additional clinical evaluations that would provide comprehensive testing of hearing, vestibular function, and visual function in USH patients. USH is also genetically heterogeneous. At least nine genes have been identified with mutations that can cause USH. The proteins encoded by these genes are thought to interact with one another to form a network in the sensory cells of the inner ear and retina.
Copyright © 2011 S. Karger AG, Basel.

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Year:  2011        PMID: 21358186     DOI: 10.1159/000322473

Source DB:  PubMed          Journal:  Adv Otorhinolaryngol        ISSN: 0065-3071


  34 in total

1.  The many faces of sensorineural hearing loss: one founder and two novel mutations affecting one family of mixed Jewish ancestry.

Authors:  Doron M Behar; Bella Davidov; Zippora Brownstein; Tamar Ben-Yosef; Karen B Avraham; Mordechai Shohat
Journal:  Genet Test Mol Biomarkers       Date:  2013-12-24

2.  Ablation of cytoskeletal scaffolding proteins, Band 4.1B and Whirlin, leads to cerebellar purkinje axon pathology and motor dysfunction.

Authors:  Julia Saifetiarova; Manzoor A Bhat
Journal:  J Neurosci Res       Date:  2018-11-17       Impact factor: 4.164

3.  In silico analysis of a disease-causing mutation in PCDH15 gene in a consanguineous Pakistani family with Usher phenotype.

Authors:  Shamim Saleha; Muhammad Ajmal; Muhammad Jamil; Muhammad Nasir; Abdul Hameed
Journal:  Int J Ophthalmol       Date:  2016-05-18       Impact factor: 1.779

Review 4.  Actin in hair cells and hearing loss.

Authors:  Meghan C Drummond; Inna A Belyantseva; Karen H Friderici; Thomas B Friedman
Journal:  Hear Res       Date:  2011-12-13       Impact factor: 3.208

5.  Inframe deletion of human ESPN is associated with deafness, vestibulopathy and vision impairment.

Authors:  Thomas J Jaworek; Gowri N Sarangdhar; Zubair M Ahmed; Lili Zheng; Khitab Gul; Shaheen N Khan; Thomas B Friedman; Robert A Sisk; James R Bartles; Sheikh Riazuddin; Saima Riazuddin
Journal:  J Med Genet       Date:  2018-03-23       Impact factor: 6.318

Review 6.  Sorting out a promiscuous superfamily: towards cadherin connectomics.

Authors:  Marcos Sotomayor; Rachelle Gaudet; David P Corey
Journal:  Trends Cell Biol       Date:  2014-04-30       Impact factor: 20.808

Review 7.  The dynamic architecture of photoreceptor ribbon synapses: cytoskeletal, extracellular matrix, and intramembrane proteins.

Authors:  Aaron J Mercer; Wallace B Thoreson
Journal:  Vis Neurosci       Date:  2011-11       Impact factor: 3.241

Review 8.  New treatment options for hearing loss.

Authors:  Ulrich Müller; Peter G Barr-Gillespie
Journal:  Nat Rev Drug Discov       Date:  2015-03-20       Impact factor: 84.694

Review 9.  The golden era of ocular disease gene discovery: race to the finish.

Authors:  A Swaroop; P A Sieving
Journal:  Clin Genet       Date:  2013-08       Impact factor: 4.438

Review 10.  [Hereditary hearing loss: Part 2: Syndromic forms of hearing loss].

Authors:  W F Burke; T Lenarz; H Maier
Journal:  HNO       Date:  2014-10       Impact factor: 1.284

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