Literature DB >> 3753284

Visual acuity loss in patients with Usher's syndrome.

L Piazza, G A Fishman, M Farber, D Derlacki, R J Anderson.   

Abstract

Using a life-table analysis, visual acuity loss with age was determined for a population of 106 patients with type 1 (N = 35) and type 2 (N = 71) Usher's syndrome. The cumulative percentage of patients maintaining visual acuity of 6/12 (20/40) or better in at least one eye by age 29 years was 69% for type 1 patients and 94% for type 2 patients. The cumulative percentage maintaining visual acuity of 6/24 (20/80) or better at this age was 89% for type 1 and 98% for type 2 patients. Within each subtype, the cumulative percentage maintaining 6/60 (20/200) or better was similar to the percentage maintaining 6/24 (20/80) or better. Knowledge of these data provides an objective basis for counseling patients with Usher's syndrome about their probability of developing loss of central visual acuity with age.

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Year:  1986        PMID: 3753284     DOI: 10.1001/archopht.1986.01050210090031

Source DB:  PubMed          Journal:  Arch Ophthalmol        ISSN: 0003-9950


  5 in total

1.  Usher syndrome in the city of Birmingham--prevalence and clinical classification.

Authors:  C I Hope; S Bundey; D Proops; A R Fielder
Journal:  Br J Ophthalmol       Date:  1997-01       Impact factor: 4.638

2.  Retinal disease course in Usher syndrome 1B due to MYO7A mutations.

Authors:  Samuel G Jacobson; Artur V Cideciyan; Dan Gibbs; Alexander Sumaroka; Alejandro J Roman; Tomas S Aleman; Sharon B Schwartz; Melani B Olivares; Robert C Russell; Janet D Steinberg; Margaret A Kenna; William J Kimberling; Heidi L Rehm; David S Williams
Journal:  Invest Ophthalmol Vis Sci       Date:  2011-10-07       Impact factor: 4.799

3.  Identification of 51 novel exons of the Usher syndrome type 2A (USH2A) gene that encode multiple conserved functional domains and that are mutated in patients with Usher syndrome type II.

Authors:  Erwin van Wijk; Ronald J E Pennings; Heleen te Brinke; Annemarie Claassen; Helger G Yntema; Lies H Hoefsloot; Frans P M Cremers; Cor W R J Cremers; Hannie Kremer
Journal:  Am J Hum Genet       Date:  2004-03-10       Impact factor: 11.025

4.  Usher syndromes due to MYO7A, PCDH15, USH2A or GPR98 mutations share retinal disease mechanism.

Authors:  Samuel G Jacobson; Artur V Cideciyan; Tomas S Aleman; Alexander Sumaroka; Alejandro J Roman; Leigh M Gardner; Haydn M Prosser; Monalisa Mishra; N Torben Bech-Hansen; Waldo Herrera; Sharon B Schwartz; Xue-Zhong Liu; William J Kimberling; Karen P Steel; David S Williams
Journal:  Hum Mol Genet       Date:  2008-05-07       Impact factor: 6.150

5.  Unravelling the pathogenic role and genotype-phenotype correlation of the USH2A p.(Cys759Phe) variant among Spanish families.

Authors:  Raquel Pérez-Carro; Fiona Blanco-Kelly; Lilián Galbis-Martínez; Gema García-García; Elena Aller; Blanca García-Sandoval; Pablo Mínguez; Marta Corton; Ignacio Mahíllo-Fernández; Inmaculada Martín-Mérida; Almudena Avila-Fernández; José M Millán; Carmen Ayuso
Journal:  PLoS One       Date:  2018-06-18       Impact factor: 3.240

  5 in total

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