Literature DB >> 6869480

Retinal function in Stargardt's disease and fundus flavimaculatus.

J B Moloney, D J Mooney, M A O'Connor.   

Abstract

Ten patients with Stargardt's disease and 14 with fundus flavimaculatus underwent thorough ophthalmic examinations, retinal photography, and, when possible, fluorescein angiography. Retinal function was also assessed by static and kinetic perimetry, the Farnsworth-Munsell 100-hue test, electro-oculography, and electroretinography. Visual acuity and color discrimination were reduced in all patients (mean visual acuity, 20/120; mean error score, 365). On electroretinography all patients had some significant abnormality of cone function and 24 eyes had abnormal rod function (mean Vmax, 298.3). Electrooculographic findings were abnormal in 24 eyes and borderline in ten others. These abnormalities were similar in both groups but more severe in fundus flavimaculatus. Stargardt's disease and fundus flavimaculatus did not co-exist in any family studied and the mean duration of disease was similar in both, indicating that Stargardt's disease did not progress to fundus flavimaculatus. Both the age of onset and duration significantly affected the severity of fundus flavimaculatus but neither had a significant effect on Stargardt's disease.

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Year:  1983        PMID: 6869480     DOI: 10.1016/0002-9394(83)90455-5

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


  17 in total

1.  Color vision in Stargardt's disease.

Authors:  M Mäntyjärvi; K Tuppurainen
Journal:  Int Ophthalmol       Date:  1992-11       Impact factor: 2.031

2.  The electroretinogram in Stargardt's disease and fundus flavimaculatus.

Authors:  P Lachapelle; J M Little; M S Roy
Journal:  Doc Ophthalmol       Date:  1989-12       Impact factor: 2.379

3.  Sorting out co-occurrence of rare monogenic retinopathies: Stargardt disease co-existing with congenital stationary night blindness.

Authors:  Nancy Huynh; Brett G Jeffrey; Amy Turriff; Paul A Sieving; Catherine A Cukras
Journal:  Ophthalmic Genet       Date:  2014-01-07       Impact factor: 1.803

4.  Stargardt's disease and fundus flavimaculatus: evaluation of morphologic progression and intrafamilial co-existence.

Authors:  T M Aaberg
Journal:  Trans Am Ophthalmol Soc       Date:  1986

Review 5.  Diagnosis and classification of macular degenerations: an approach based on retinal function testing.

Authors:  L Scullica; B Falsini
Journal:  Doc Ophthalmol       Date:  2001-05       Impact factor: 2.379

6.  Stargardt's disease. Family studies.

Authors:  M Mäntyjärvi; K Tuppurainen
Journal:  Doc Ophthalmol       Date:  1992       Impact factor: 2.379

7.  Stargardt's disease/fundus flavimaculatus: psychophysical and electrophysiologic results.

Authors:  R Itabashi; O Katsumi; M C Mehta; R Wajima; M Tamai; T Hirose
Journal:  Graefes Arch Clin Exp Ophthalmol       Date:  1993-10       Impact factor: 3.117

8.  Clinical phenotypes and prognostic full-field electroretinographic findings in Stargardt disease.

Authors:  Sarwar Zahid; Thiran Jayasundera; William Rhoades; Kari Branham; Naheed Khan; Leslie M Niziol; David C Musch; John R Heckenlively
Journal:  Am J Ophthalmol       Date:  2012-12-05       Impact factor: 5.258

9.  A gene for late-onset fundus flavimaculatus with macular dystrophy maps to chromosome 1p13.

Authors:  S Gerber; J M Rozet; D Bonneau; E Souied; A Camuzat; J L Dufier; P Amalric; J Weissenbach; A Munnich; J Kaplan
Journal:  Am J Hum Genet       Date:  1995-02       Impact factor: 11.025

10.  A YAC contig encompassing the recessive Stargardt disease gene (STGD) on chromosome 1p.

Authors:  K L Anderson; L Baird; R A Lewis; A C Chinault; B Otterud; M Leppert; J R Lupski
Journal:  Am J Hum Genet       Date:  1995-12       Impact factor: 11.025

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