Literature DB >> 7377267

Visual loss in retinitis pigmentosa.

M F Marmor.   

Abstract

I investigated the visual histories of 91 consecutive patients with retinitis pigmentosa to determine when, and how fast, visual acuity was affected by the disease. The results from recessive cases showed that visual loss may occur at any age in retinitis pigmentosa, and typically progresses from 6/12 (20/40) to 6/60 (20/200) in about six years. At any given time, most of the patients had either good or poor visual acuity; intermediate levels of visual acuity appeared to be unstable. Before age 20 years, 60 to 90% of the patients had a visual acuity of 6/12 (20/40) or better, and few had a visual acuity of 6/60 (20/200) or worse. By age 50 years, 25% of the patients still retained good visual acuity, but more than 50% had visual acuity of 6/60 (20/200) or worse.

Entities:  

Mesh:

Year:  1980        PMID: 7377267     DOI: 10.1016/0002-9394(80)90289-5

Source DB:  PubMed          Journal:  Am J Ophthalmol        ISSN: 0002-9394            Impact factor:   5.258


  13 in total

1.  L- and M-cone driven large-field and multifocal electroretinograms in sector retinitis pigmentosa.

Authors:  Hendrik P N Scholl; Jan Kremers
Journal:  Doc Ophthalmol       Date:  2003-03       Impact factor: 2.379

2.  Test-retest reliability of the multifocal electroretinogram and humphrey visual fields in patients with retinitis pigmentosa.

Authors:  William Seiple; Colleen J Clemens; Vivienne C Greenstein; Ronald E Carr; Karen Holopigian
Journal:  Doc Ophthalmol       Date:  2004-11       Impact factor: 2.379

3.  Correlations between electroretinography, morphology and function in retinitis pigmentosa.

Authors:  M Fahle; K P Steuhl; E Aulhorn
Journal:  Graefes Arch Clin Exp Ophthalmol       Date:  1991       Impact factor: 3.117

4.  Visual acuity loss in recessive retinitis pigmentosa and its correlation with macular lesions.

Authors:  Azzrah Thobani; Gerald A Fishman; Mohamed Genead; Anastasios Anastasakis
Journal:  Retina       Date:  2011-05       Impact factor: 4.256

5.  Longitudinal Clinical Follow-up and Genetic Spectrum of Patients With Rod-Cone Dystrophy Associated With Mutations in PDE6A and PDE6B.

Authors:  Samer Khateb; Marco Nassisi; Kinga M Bujakowska; Cécile Méjécase; Christel Condroyer; Aline Antonio; Marine Foussard; Vanessa Démontant; Saddek Mohand-Saïd; José-Alain Sahel; Christina Zeitz; Isabelle Audo
Journal:  JAMA Ophthalmol       Date:  2019-06-01       Impact factor: 7.389

6.  Blindness and visual impairment in retinitis pigmentosa: a Cameroonian hospital-based study.

Authors:  André Omgbwa Eballe; Godefroy Koki; Claude Bernard Emche; Lucienne Assumpta Bella; Jeanne Mayouego Kouam; Justin Melong
Journal:  Clin Ophthalmol       Date:  2010-07-30

7.  An epidemiological approach for the estimation of disease onset in Central Europe in central and peripheral monogenic retinal dystrophies.

Authors:  Elena Prokofyeva; Robert Wilke; Gunnar Lotz; Eric Troeger; Torsten Strasser; Eberhart Zrenner
Journal:  Graefes Arch Clin Exp Ophthalmol       Date:  2009-03-11       Impact factor: 3.117

8.  Pattern-reversal electroretinograms and visual evoked potentials in retinitis pigmentosa.

Authors:  Márta Janáky; Andrea Pálffy; Gyöngyi Horváth; Gábor Tuboly; György Benedek
Journal:  Doc Ophthalmol       Date:  2007-11-22       Impact factor: 2.379

9.  RP cone-rod degeneration.

Authors:  J R Heckenlively
Journal:  Trans Am Ophthalmol Soc       Date:  1987

10.  Equivalent intrinsic noise, sampling efficiency, and contrast sensitivity in patients with retinitis pigmentosa.

Authors:  J Jason McAnany; Kenneth R Alexander; Mohamed A Genead; Gerald A Fishman
Journal:  Invest Ophthalmol Vis Sci       Date:  2013-06-03       Impact factor: 4.799

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