Literature DB >> 9693297

Unilateral retinitis pigmentosa: clinical and electrophysiological report of four cases.

L Spadea1, R Magni, G Rinaldi, T Dragani, G Bianco.   

Abstract

Unilateral retinitis pigmentosa (URP) is a rare tapetoretinal dystrophy affecting only one eye. The François and Verriest criteria are necessary to make a correct diagnosis of URP: exclude all infective etiologies, check that the clinical signs of retinitis are present in the affected eye and ensure the total absence of any signs or symptoms of retinitis pigmentosa in the fellow eye. The standard electroretinogram and standard electro-oculogram are very useful for the correct diagnosis. Other pigmentary retinopathies simulating retinitis pigmentosa have to be excluded, such as previous retinal inflammatory diseases like syphilis, rubeola, other viral diseases and onchocerciasis. In this paper, 4 cases of URP are reported.

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Year:  1998        PMID: 9693297     DOI: 10.1159/000027324

Source DB:  PubMed          Journal:  Ophthalmologica        ISSN: 0030-3755            Impact factor:   3.250


  3 in total

1.  Disease course of patients with unilateral pigmentary retinopathy.

Authors:  Emorfily Potsidis; Eliot L Berson; Michael A Sandberg
Journal:  Invest Ophthalmol Vis Sci       Date:  2011-11-29       Impact factor: 4.799

2.  Unilateral retinitis pigmentosa with amblyopia in the fellow eye.

Authors:  Hongling Chen; Dezheng Wu; Shizhou Huang; Futian Jiang
Journal:  Graefes Arch Clin Exp Ophthalmol       Date:  2006-12       Impact factor: 3.117

3.  A Case of Unilateral Retinitis Pigmentosa Associated with Full Thickness Macular Hole.

Authors:  Lama Enani; Igor Kozak; Ehab Abdelkader
Journal:  Middle East Afr J Ophthalmol       Date:  2017 Apr-Jun
  3 in total

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