Literature DB >> 15790919

Cone and rod dysfunction in fundus albipunctatus with RDH5 mutation: an electrophysiological study.

Yasuhiro Niwa1, Mineo Kondo, Shinji Ueno, Makoto Nakamura, Hiroko Terasaki, Yozo Miyake.   

Abstract

PURPOSE: A prior study showed that some patients with fundus albipunctatus (FA) have severely reduced full-field cone ERGs. The purpose of this study was to investigate the frequency of cone dysfunction and to determine the cause of the reduced full-field cone ERGs in patients with FA and whether the rod system is affected in patients with FA.
METHODS: Sixteen consecutive patients with FA (from 1993 to 2003; eight males, eight females; mean age, 25.4 years) with an RDH5 gene mutation were studied. The amplitudes and implicit times of the standard cone ERGs in the patients with FA were compared to those obtained from normal subjects (n = 55). The a-waves of cone ERGs were also elicited by a bright flash and were fitted to a mathematical model of the a-wave. Rod ERG responses were elicited by dim blue flashes after 3 hours of dark adaptation.
RESULTS: The amplitude of the b-wave of the cone ERG in the FA group varied considerably from within the normal limits to markedly decreased. Six of 16 patients with FA had b-wave amplitudes that were smaller than the lowest limit of the control subjects. The degree of cone dysfunction tended to be more severe in older patients. The analysis of the cone a-wave demonstrated that R(m) (maximal response amplitude) in the patients with FA with reduced standard cone ERGs was significantly smaller than that in control subjects. Rod ERGs were also reduced in the patients with FA who had reduced cone ERGs.
CONCLUSIONS: In patients with FA, 38% had extensive cone dysfunction. The reduced full-field cone ERGs were mainly due to the loss of cone photoreceptors, and the rod system was also affected in some patients.

Entities:  

Mesh:

Substances:

Year:  2005        PMID: 15790919     DOI: 10.1167/iovs.04-0638

Source DB:  PubMed          Journal:  Invest Ophthalmol Vis Sci        ISSN: 0146-0404            Impact factor:   4.799


  21 in total

Review 1.  Multimodal fundus imaging in fundus albipunctatus with RDH5 mutation: a newly identified compound heterozygous mutation and review of the literature.

Authors:  Nan-Kai Wang; Lan-Hsin Chuang; Chi-Chun Lai; Chai Lin Chou; Hsueh-Yen Chu; Ling Yeung; Yen-Po Chen; Kuan-Jen Chen; Wei-Chi Wu; Tun-Lu Chen; An-Ning Chao; Yih-Shiou Hwang
Journal:  Doc Ophthalmol       Date:  2012-06-06       Impact factor: 2.379

Review 2.  The retinal pigment epithelium in health and disease.

Authors:  J R Sparrow; D Hicks; C P Hamel
Journal:  Curr Mol Med       Date:  2010-12       Impact factor: 2.222

Review 3.  Recent advances in the dark adaptation investigations.

Authors:  Guo-Qing Yang; Tao Chen; Ye Tao; Zuo-Ming Zhang
Journal:  Int J Ophthalmol       Date:  2015-12-18       Impact factor: 1.779

4.  Late-onset night blindness with peripheral flecks accompanied by progressive trickle-like macular degeneration.

Authors:  Kazushige Tsunoda; Kaoru Fujinami; Kazutoshi Yoshitake; Takeshi Iwata
Journal:  Doc Ophthalmol       Date:  2019-07-08       Impact factor: 2.379

Review 5.  The use of SD-OCT in the differential diagnosis of dots, spots and other white retinal lesions.

Authors:  Elena Zaharova; Jerome Sherman
Journal:  Eye Brain       Date:  2011-10-25

6.  exomeSuite: Whole exome sequence variant filtering tool for rapid identification of putative disease causing SNVs/indels.

Authors:  B Maranhao; P Biswas; J L Duncan; K E Branham; G A Silva; M A Naeem; S N Khan; S Riazuddin; J F Hejtmancik; J R Heckenlively; S A Riazuddin; P L Lee; R Ayyagari
Journal:  Genomics       Date:  2014-03-03       Impact factor: 5.736

7.  Improvement in rod and cone function in mouse model of Fundus albipunctatus after pharmacologic treatment with 9-cis-retinal.

Authors:  Akiko Maeda; Tadao Maeda; Krzysztof Palczewski
Journal:  Invest Ophthalmol Vis Sci       Date:  2006-10       Impact factor: 4.799

8.  Fundus albipunctatus in a 6-year old girl due to compound heterozygous mutations in the RDH5 gene.

Authors:  Alessandro Iannaccone; Salvatore A Tedesco; Kevin T Gallaher; Hiroyuki Yamamoto; Steve Charles; Thaddeus P Dryja
Journal:  Doc Ophthalmol       Date:  2007-05-03       Impact factor: 2.379

9.  Diagnosis in a patient with fundus albipunctatus and atypical fundus changes.

Authors:  Manal Hajali; Gerald A Fishman; Thaddeus P Dryja; Meredith O Sweeney; Martin Lindeman
Journal:  Doc Ophthalmol       Date:  2008-10-24       Impact factor: 2.379

10.  A novel mutation in RDH5 gene causes retinitis pigmentosa in consanguineous Pakistani family.

Authors:  Neelam Sultan; Irfan Ali; Shazia Anwer Bukhari; Shahid Mahmood Baig; Muhammad Asif; Muhammad Qasim; Muhammad Imran Naseer; Mahmood Rasool
Journal:  Genes Genomics       Date:  2018-02-03       Impact factor: 1.839

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.