 |
 |

Shared Mutations in NR2E3 in Enhanced S-cone Syndrome, Goldmann-Favre Syndrome, and Many Cases of Clumped Pigmentary Retinal Degeneration
Dror Sharon, PhD;
Michael A. Sandberg, PhD;
Rafael C. Caruso, MD;
Eliot L. Berson, MD;
Thaddeus P. Dryja, MD
Arch Ophthalmol. 2003;121:1316-1323.
Objectives To determine if enhanced s-cone syndrome (ESCS), Goldmann-Favre syndrome (GFS), and clumped pigmentary retinal degeneration (CPRD) are caused by mutations in the NR2E3 gene and to characterize the clinical findings in patients with NR2E3 mutations.
Patients One patient with ESCS, one with GFS, and 20 with CPRD.
Methods The coding regions of the NR2E3 and NRL genes and part of the THRB1 coding region were scanned for mutations using single-strand conformation and direct sequencing methods. We evaluated visual acuity, refractive error, visual fields, fundi, final dark-adaptation thresholds, and electroretinograms (ERGs).
Results The patients with ESCS and GFS and 9 of the 20 unrelated patients with CPRD had mutations in the NR2E3 gene. Six mutations were found in these 11 patients, including 2 novel mutations: the missense mutation Ala256Glu and the frameshift mutation Pro276del17 (the first obviously null allele reported). Three patients were mutant homozygotes, and 8 had 2 mutations. All but one of the mutations in the patients with ESCS and GFS were also found in patients with CPRD. All NR2E3 cases were hyperopes and had retinal vascular attenuation and reduced and delayed full-field ERGs. Clumped pigment deposits were recognized in the patients with ESCS and GFS. The CPRD patients without NR2E3 mutations had no detected mutations in NRL or THRB1.
Conclusions We found that ESCS, GFS, and CPRD can all have the same genetic basis.
Clinical Relevance The combination of night blindness, hyperopia, and clumped retinal pigment deposits should raise the suspicion that a patient has NR2E3 disease.
From the Ocular Molecular Genetics Institute and the Berman-Gund Laboratory for the Study of Retinal Degenerations, Harvard Medical School, Massachusetts Eye and Ear Infirmary, Boston (Drs Sharon, Sandberg, Berson, and Dryja); and the National Eye Institute, Bethesda, Md (Dr Caruso). Dr Sharon is now with the Department of Ophthalmology, Hadassah Medical Organization, Jerusalem, Israel. The authors have no relevant financial interest in this article.
CiteULike Connotea Del.icio.us Digg Reddit Technorati Twitter
What's this?
THIS ARTICLE HAS BEEN CITED BY OTHER ARTICLES
 |
Cellular origin of fundus autofluorescence in patients and mice with a defective NR2E3 gene
Wang et al.
Br J Ophthalmol 2009;93:1234-1240.
ABSTRACT
| FULL TEXT
The enhanced S-cone syndrome in children
Khan et al.
BMJ Case Reports 2009;2009:bcr1020081163-bcr1020081163.
ABSTRACT
| FULL TEXT
The Spectrum of Retinal Diseases Caused by NR2E3 Mutations in Israeli and Palestinian Patients
Bandah et al.
Arch Ophthalmol 2009;127:297-302.
ABSTRACT
| FULL TEXT
Phenotypic Features of Patients With NR2E3 Mutations
Pachydaki et al.
Arch Ophthalmol 2009;127:71-75.
ABSTRACT
| FULL TEXT
Phenotypic Variation in Enhanced S-cone Syndrome
Audo et al.
IOVS 2008;49:2082-2093.
ABSTRACT
| FULL TEXT
Bilateral giant macular schisis in a patient with enhanced S-cone syndrome from a family showing pseudo-dominant inheritance
Vaclavik et al.
Br J Ophthalmol 2008;92:299-300.
FULL TEXT
X-linked retinoschisis: an update
Sikkink et al.
J. Med. Genet. 2007;44:225-232.
ABSTRACT
| FULL TEXT
The enhanced S-cone syndrome in children
Khan et al.
Br J Ophthalmol 2007;91:394-396.
FULL TEXT
In vivo function of the orphan nuclear receptor NR2E3 in establishing photoreceptor identity during mammalian retinal development
Cheng et al.
Hum Mol Genet 2006;15:2588-2602.
ABSTRACT
| FULL TEXT
Human blue-opsin promoter preferentially targets reporter gene expression to rat s-cone photoreceptors.
Glushakova et al.
IOVS 2006;47:3505-3513.
ABSTRACT
| FULL TEXT
Effects of L1 retrotransposon insertion on transcript processing, localization and accumulation: lessons from the retinal degeneration 7 mouse and implications for the genomic ecology of L1 elements
Chen et al.
Hum Mol Genet 2006;15:2146-2156.
ABSTRACT
| FULL TEXT
An Arg311Gln NR2E3 mutation in a family with classic Goldmann-Favre syndrome
Chavala et al.
Br J Ophthalmol 2005;89:1065-1066.
FULL TEXT
Identification of regulatory targets of tissue-specific transcription factors: application to retina-specific gene regulation
Qian et al.
Nucleic Acids Res 2005;33:3479-3491.
ABSTRACT
| FULL TEXT
The Rod Photoreceptor-Specific Nuclear Receptor Nr2e3 Represses Transcription of Multiple Cone-Specific Genes
Chen et al.
J. Neurosci. 2005;25:118-129.
ABSTRACT
| FULL TEXT
Recessive NRL mutations in patients with clumped pigmentary retinal degeneration and relative preservation of blue cone function
Nishiguchi et al.
Proc. Natl. Acad. Sci. USA 2004;101:17819-17824.
ABSTRACT
| FULL TEXT
Nuclear receptor NR2E3 gene mutations distort human retinal laminar architecture and cause an unusual degeneration
Jacobson et al.
Hum Mol Genet 2004;13:1893-1902.
ABSTRACT
| FULL TEXT
Photoreceptor-specific nuclear receptor NR2E3 functions as a transcriptional activator in rod photoreceptors
Cheng et al.
Hum Mol Genet 2004;13:1563-1575.
ABSTRACT
| FULL TEXT
|