Literature DB >> 17102007

Localization of multifocal electroretinogram abnormalities to the lesion site: findings in a family with Best disease.

Inna V Glybina1, Robert N Frank.   

Abstract

OBJECTIVE: To determine the association between multifocal electroretinogram (mfERG) abnormalities and macular lesions, as shown by retinal photography and optical coherence tomography (OCT), in a 3-generation family with vitelliform macular dystrophy.
METHODS: Five family members were examined using OCT, mfERG, and retinal photography. To localize mfERG abnormalities in relation to retinal findings, we overlaid the mfERG trace arrays on the retinal images and aligned the mfERGs and OCT images in the 180 degrees meridian.
RESULTS: Family members had typical macular lesions, normal full-field ERGs, and reduced electro-oculogram light-dark ratios. The OCT images demonstrated variable lesion severity. Some individuals with good vision and normal-appearing fundi showed OCT abnormalities of the choroid and retinal pigment epithelium. The overlay technique revealed that the depressed mfERGs corresponded with the lesions detected by OCT and retinal photography. The latencies of mfERG components in the 2 central stimulus rings in our patients were often prolonged.
CONCLUSIONS: The mfERG abnormalities matched the localization of the macular lesions in our patients. The latencies of the mfERG N1 and P1 components in the first 2 concentric stimulus rings were often significantly (>2 SDs) delayed, an observation that has not been previously reported, to our knowledge.

Entities:  

Mesh:

Year:  2006        PMID: 17102007     DOI: 10.1001/archopht.124.11.1593

Source DB:  PubMed          Journal:  Arch Ophthalmol        ISSN: 0003-9950


  6 in total

1.  Multimodal fundus imaging in Best vitelliform macular dystrophy.

Authors:  Daniela C Ferrara; Rogério A Costa; Stephen Tsang; Daniela Calucci; Rodrigo Jorge; K Bailey Freund
Journal:  Graefes Arch Clin Exp Ophthalmol       Date:  2010-04-23       Impact factor: 3.117

2.  Quantitative fundus autofluorescence and optical coherence tomography in best vitelliform macular dystrophy.

Authors:  Tobias Duncker; Jonathan P Greenberg; Rithambara Ramachandran; Donald C Hood; R Theodore Smith; Tatsuo Hirose; Russell L Woods; Stephen H Tsang; François C Delori; Janet R Sparrow
Journal:  Invest Ophthalmol Vis Sci       Date:  2014-03-13       Impact factor: 4.799

3.  Best macular dystrophy in a nigerian: a case report.

Authors:  Tunji S Oluleye
Journal:  Case Rep Ophthalmol       Date:  2012-06-12

4.  Phenotypic variability in a French family with a novel mutation in the BEST1 gene causing multifocal best vitelliform macular dystrophy.

Authors:  Emmanuelle Lacassagne; Aurore Dhuez; Florence Rigaudière; Anouk Dansault; Christelle Vêtu; Karine Bigot; Véronique Vieira; Bernard Puech; Sabine Defoort-Dhellemmes; Marc Abitbol
Journal:  Mol Vis       Date:  2011-01-29       Impact factor: 2.367

5.  PHOTORECEPTOR INNER SEGMENT MORPHOLOGY IN BEST VITELLIFORM MACULAR DYSTROPHY.

Authors:  Drew Scoles; Yusufu N Sulai; Robert F Cooper; Brian P Higgins; Ryan D Johnson; Joseph Carroll; Alfredo Dubra; Kimberly E Stepien
Journal:  Retina       Date:  2017-04       Impact factor: 4.256

6.  Combination of Multifocal Electroretinogram and Spectral-Domain OCT Can Increase Diagnostic Efficacy of Parkinson's Disease.

Authors:  Jiang Huang; Yi Li; Jianjiang Xiao; Qin Zhang; Guoxu Xu; Guanhui Wu; Tong Liu; Weifeng Luo
Journal:  Parkinsons Dis       Date:  2018-03-01
  6 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.