Literature DB >> 14986011

Novel 473-bp deletion in XLRS1 gene in a Japanese family with X-linked juvenile retinoschisis.

Kei Shinoda1, Hisao Ohde, Susumu Ishida, Makoto Inoue, Yoshihisa Oguchi, Yukihiko Mashima.   

Abstract

PURPOSE: To present the clinical features of two brothers with molecularly confirmed X-linked juvenile retinoschisis (xlRS) but with non-characteristic electrophysiological findings.
METHODS: Comprehensive ophthalmological examinations were performed. The electroretinograms (ERGs) were recorded under ISCEV standards, and ERGs elicited by long-duration stimuli were also evaluated. Standard genetic analysis of peripheral blood leukocytes was performed.
RESULTS: Molecular testing revealed a novel 473-bp deletion including exon 4 in the XLRS1 gene in both siblings. This resulted in a frameshift mutation and a premature termination at codon 78. The scotopic and photopic ERGs were reduced, but the "negative-type" ERG, characteristic of xlRS, was not observed. Flicker ERGs were also highly reduced. Long-duration stimuli elicited ERGs with a complete loss of the b-wave and a preservation of the off-response, i.e., negative-type ERG. The phenotype/genotype relationship was not determined.
CONCLUSION: The consistency of the ERGs elicited by long-duration stimuli in xlRS patients suggests that this type of stimuli provides responses that are a better indicator for the progression or stage of the disease.

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Year:  2004        PMID: 14986011     DOI: 10.1007/s00417-004-0878-y

Source DB:  PubMed          Journal:  Graefes Arch Clin Exp Ophthalmol        ISSN: 0721-832X            Impact factor:   3.117


  27 in total

1.  On-response deficit in the electroretinogram of the cone system in X-linked retinoschisis.

Authors:  K R Alexander; G A Fishman; C S Barnes; S Grover
Journal:  Invest Ophthalmol Vis Sci       Date:  2001-02       Impact factor: 4.799

2.  X-linked congenital retinoschisis.

Authors:  U Kellner; S Brümmer; M H Foerster; A Wessing
Journal:  Graefes Arch Clin Exp Ophthalmol       Date:  1990       Impact factor: 3.117

3.  Positional cloning of the gene associated with X-linked juvenile retinoschisis.

Authors:  C G Sauer; A Gehrig; R Warneke-Wittstock; A Marquardt; C C Ewing; A Gibson; B Lorenz; B Jurklies; B H Weber
Journal:  Nat Genet       Date:  1997-10       Impact factor: 38.330

4.  Pathology of hereditary juvenile retinoschisis.

Authors:  W A Manschot
Journal:  Arch Ophthalmol       Date:  1972-08

5.  On- and off-responses of the photopic electroretinograms in X-linked juvenile retinoschisis.

Authors:  K Shinoda; H Ohde; Y Mashima; R Inoue; S Ishida; M Inoue; S Kawashima; Y Oguchi
Journal:  Am J Ophthalmol       Date:  2001-04       Impact factor: 5.258

6.  Clinical characteristics of 14 japanese patients with X-linked juvenile retinoschisis associated with XLRS1 mutation.

Authors:  K Shinoda; S Ishida; Y Oguchi; Y Mashima
Journal:  Ophthalmic Genet       Date:  2000-09       Impact factor: 1.803

7.  Indications for vitrectomy in congenital retinoschisis.

Authors:  J Schulman; G A Peyman; N Jednock; B Larson
Journal:  Br J Ophthalmol       Date:  1985-07       Impact factor: 4.638

8.  Infantile presentation of X linked retinoschisis.

Authors:  N D George; J R Yates; K Bradshaw; A T Moore
Journal:  Br J Ophthalmol       Date:  1995-07       Impact factor: 4.638

9.  Mutations of the XLRS1 gene cause abnormalities of photoreceptor as well as inner retinal responses of the ERG.

Authors:  K Bradshaw; N George; A Moore; D Trump
Journal:  Doc Ophthalmol       Date:  1999       Impact factor: 1.854

10.  Clinical features of X linked juvenile retinoschisis associated with new mutations in the XLRS1 gene in Italian families.

Authors:  F Simonelli; G Cennamo; C Ziviello; F Testa; G de Crecchio; A Nesti; M P Manitto; A Ciccodicola; S Banfi; R Brancato; E Rinaldi
Journal:  Br J Ophthalmol       Date:  2003-09       Impact factor: 4.638

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  6 in total

1.  Mutations in the XLRS1 gene in Thai families with X-linked juvenile retinoschisis.

Authors:  La-ongsri Atchaneeyasakul; Adisak Trinavarat; Auengporn Pituksung; Worapoj Jinda; Wanna Thongnoppakhun; Chanin Limwongse
Journal:  Jpn J Ophthalmol       Date:  2010-02-12       Impact factor: 2.447

2.  Molecular mechanisms leading to null-protein product from retinoschisin (RS1) signal-sequence mutants in X-linked retinoschisis (XLRS) disease.

Authors:  Camasamudram Vijayasarathy; Ruifang Sui; Yong Zeng; Guoxing Yang; Fei Xu; Rafael C Caruso; Richard A Lewis; Lucia Ziccardi; Paul A Sieving
Journal:  Hum Mutat       Date:  2010-11       Impact factor: 4.878

3.  Null retinoschisin-protein expression from an RS1 c354del1-ins18 mutation causing progressive and severe XLRS in a cross-sectional family study.

Authors:  Camasamudram Vijayasarathy; Lucia Ziccardi; Yong Zeng; Nizar Smaoui; Rafael C Caruso; Paul A Sieving
Journal:  Invest Ophthalmol Vis Sci       Date:  2009-05-27       Impact factor: 4.799

4.  Truncation of retinoschisin protein associated with a novel splice site mutation in the RS1 gene.

Authors:  Balázs Lesch; Viktória Szabó; Melinda Kánya; Balázs Varsányi; Gábor M Somfai; János Hargitai; Rita Vámos; Orsolya Fiedler; Agnes Farkas
Journal:  Mol Vis       Date:  2008-08-25       Impact factor: 2.367

5.  Clinical and genetic findings in Hungarian patients with X-linked juvenile retinoschisis.

Authors:  B Lesch; V Szabó; M Kánya; G M Somfai; R Vámos; B Varsányi; Zs Pámer; K Knézy; Gy Salacz; M Janáky; M Ferencz; J Hargitai; A Papp; A Farkas
Journal:  Mol Vis       Date:  2008-12-12       Impact factor: 2.367

6.  ISCEV extended protocol for the photopic On-Off ERG.

Authors:  Maja Sustar; Graham E Holder; Jan Kremers; Claire S Barnes; Bo Lei; Naheed W Khan; Anthony G Robson
Journal:  Doc Ophthalmol       Date:  2018-06-22       Impact factor: 2.379

  6 in total

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