Literature DB >> 16879578

Longterm visual prognosis in Usher syndrome types 1 and 2.

André M Sadeghi1, Kristina Eriksson, William J Kimberling, Anders Sjöström, Claes Möller.   

Abstract

PURPOSE: To estimate the age at diagnosis of retinitis pigmentosa and to determine visual acuity deterioration, visual field impairment and the frequency of cataracts in Usher syndrome types 1 and 2.
METHODS: We carried out a retrospective study of 328 affected subjects with Usher syndrome types 1 and 2. Study subjects were divided into seven different age groups by decade. Data were analysed using descriptive statistics, general linear model anova and survival analysis.
RESULTS: Retinitis pigmentosa was diagnosed significantly earlier in subjects with Usher syndrome type 1 than in those with type 2. Visual acuity was significantly more impaired in affected subjects with Usher syndrome type 1 than in those with type 2 from 50 years of age onwards. Survival analysis revealed a significant difference in visual field loss (<or= 10 degrees) between the two groups, with type 2 subjects tending to be more impaired, while comparison indicated no significant differences between the groups in any of the other visual field categories. Cataract was found to be generally more common in Usher syndrome type 1 than type 2.
CONCLUSIONS: Progressive loss of visual acuity and visual field begins to be substantial between the second and third decades of life in both Usher types. The rate of degeneration varies between individuals in both groups. The data are useful for the counselling of affected subjects with Usher syndrome types 1 and 2.

Entities:  

Mesh:

Year:  2006        PMID: 16879578     DOI: 10.1111/j.1600-0420.2006.00675.x

Source DB:  PubMed          Journal:  Acta Ophthalmol Scand        ISSN: 1395-3907


  11 in total

1.  Relationship between foveal cone structure and clinical measures of visual function in patients with inherited retinal degenerations.

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Journal:  Invest Ophthalmol Vis Sci       Date:  2013-08-28       Impact factor: 4.799

2.  Cone responses in Usher syndrome types 1 and 2 by microvolt electroretinography.

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3.  Hearing impairment caused by mutations in two different genes responsible for nonsyndromic and syndromic hearing loss within a single family.

Authors:  Katarzyna Niepokój; Agnieszka M Rygiel; Piotr Jurczak; Aleksandra A Kujko; Dominika Śniegórska; Justyna Sawicka; Alicja Grabarczyk; Jerzy Bal; Katarzyna Wertheim-Tysarowska
Journal:  J Appl Genet       Date:  2017-11-18       Impact factor: 3.240

4.  Current understanding of usher syndrome type II.

Authors:  Jun Yang; Le Wang; Hongman Song; Maxim Sokolov
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Review 5.  Correction of Monogenic and Common Retinal Disorders with Gene Therapy.

Authors:  Jesse D Sengillo; Sally Justus; Thiago Cabral; Stephen H Tsang
Journal:  Genes (Basel)       Date:  2017-01-27       Impact factor: 4.096

6.  Visual Field Progression in Retinitis Pigmentosa.

Authors:  Manlong Xu; Yi Zhai; Ian M MacDonald
Journal:  Invest Ophthalmol Vis Sci       Date:  2020-06-03       Impact factor: 4.799

7.  The lived experiences of work and health of people living with deaf-blindness due to Usher syndrome type 2.

Authors:  Mattias Ehn; Moa Wahlqvist; Claes Möller; Agneta Anderzén-Carlsson
Journal:  Int J Qual Stud Health Well-being       Date:  2020-12

Review 8.  Usher Syndrome.

Authors:  Alessandro Castiglione; Claes Möller
Journal:  Audiol Res       Date:  2022-01-11

9.  Visual function and ocular status of children with hearing impairment in Oman: a case series.

Authors:  Rajiv Khandekar; Mohammed Al Fahdi; Bushra Al Jabri; Saleh Al Harby; Talat Abdulamgeed
Journal:  Indian J Ophthalmol       Date:  2009 May-Jun       Impact factor: 1.848

10.  Clarin-1 expression in adult mouse and human retina highlights a role of Müller glia in Usher syndrome.

Authors:  Lei Xu; Susan N Bolch; Clayton P Santiago; Frank M Dyka; Omar Akil; Ekaterina S Lobanova; Yuchen Wang; Kirill A Martemyanov; William W Hauswirth; W Clay Smith; James T Handa; Seth Blackshaw; John D Ash; Astra Dinculescu
Journal:  J Pathol       Date:  2019-12-04       Impact factor: 7.996

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