Literature DB >> 12678279

Detection of retinal dysfunction in vitelliform macular dystrophy using the multifocal ERG (MF-ERG).

Anja M Palmowski1, Reiner Allgayer, Bernhild Heinemann-Vernaleken, Volker Scherer, Klaus W Ruprecht.   

Abstract

Vitelliform macular dystrophy (VMD) is widely known for an abnormal EOG in the presence of a normal ERG. In this study the multifocal electroretinogram (MF-ERG) is described as an additional tool to detect retinal dysfunction in VMD. Three patients aged 30, 37 and 59 years with VMD and a visual acuity of OD: 0.4; OS 0.05 (patient 1), 1.25 OU (patient 2) and OU: 0.6 (patient 3) underwent additional electrophysiological testing with the MF-ERG. A multifocal-ERG of the central 50 degrees of the retina was obtained using the VERIS-system. During recording 103 hexagons flickered according to a binary m-sequence of 2(15). Mean luminance was 100 cd/m2, contrast was set at 99%. The MF-ERG recordings were compared to age matched control groups. In all three patients the MF-ERG of the central 6 degrees showed reduced amplitudes for N1P1 (first negative peak to first positive peak) and for P1N2 (P1 to the second negative peak). Implicit times were not affected. Therefore the MF-ERG can detect focal retinal dysfunction in VMD which would not be apparent in the summed retinal response recorded with the ganzfeld ERG. In contrast to other diseases, amplitudes rather than implicit times seem to be affected in the MF-ERG of vitelliform macular dystrophy.

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Year:  2003        PMID: 12678279     DOI: 10.1023/a:1022550008074

Source DB:  PubMed          Journal:  Doc Ophthalmol        ISSN: 0012-4486            Impact factor:   2.379


  16 in total

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2.  Multifocal electroretinography in patients with Stargardt's macular dystrophy.

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Review 4.  VMD2 mutations in vitelliform macular dystrophy (Best disease) and other maculopathies.

Authors:  K White; A Marquardt; B H Weber
Journal:  Hum Mutat       Date:  2000       Impact factor: 4.878

5.  Electro-oculography in families with vitelliform dystrophy of the fovea. Detection of the carrier state.

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Journal:  Arch Ophthalmol       Date:  1969-03

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Authors:  U Kretschmann; R Stilling; K Rüther; E Zrenner
Journal:  Graefes Arch Clin Exp Ophthalmol       Date:  1999-05       Impact factor: 3.117

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Journal:  Ophthalmologe       Date:  1999-03       Impact factor: 1.059

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Journal:  Ophthalmologica       Date:  1999       Impact factor: 3.250

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Authors:  E M Stone; B E Nichols; L M Streb; A E Kimura; V C Sheffield
Journal:  Nat Genet       Date:  1992-07       Impact factor: 38.330

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  3 in total

Review 1.  Bestrophin 1 and retinal disease.

Authors:  Adiv A Johnson; Karina E Guziewicz; C Justin Lee; Ravi C Kalathur; Jose S Pulido; Lihua Y Marmorstein; Alan D Marmorstein
Journal:  Prog Retin Eye Res       Date:  2017-01-30       Impact factor: 21.198

2.  New VMD2 gene mutations identified in patients affected by Best vitelliform macular dystrophy.

Authors:  D Marchant; K Yu; K Bigot; O Roche; A Germain; D Bonneau; V Drouin-Garraud; D F Schorderet; F Munier; D Schmidt; P Le Neindre; C Marsac; M Menasche; J L Dufier; R Fischmeister; C Hartzell; M Abitbol
Journal:  J Med Genet       Date:  2007-02-07       Impact factor: 6.318

3.  BEST1 sequence variants in Italian patients with vitelliform macular dystrophy.

Authors:  Andrea Sodi; Ilaria Passerini; Vittoria Murro; Roberto Caputo; Giacomo Maria Bacci; Mirela Bodoj; Francesca Torricelli; Ugo Menchini
Journal:  Mol Vis       Date:  2012-11-17       Impact factor: 2.367

  3 in total

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