 |
|
X-Linked Retinoschisis With Point Mutations in the XLRS1 Gene
Yumiko Inoue, MD;
Shuji Yamamoto, MD;
Masaki Okada, MD;
Motokazu Tsujikawa, MD;
Tomoyuki Inoue, MD;
Annabelle A. Okada, MD;
Shunji Kusaka, MD;
Yoshihiro Saito, MD;
Kenji Wakabayashi, MD;
Yozo Miyake, MD;
Takashi Fujikado, MD;
Yasuo Tano, MD
Arch Ophthalmol. 2000;118:93-96.
Background X-linked retinoschisis (XLRS) is a relatively rare vitreoretinal dystrophy that causes visual loss in young men. Recently, a gene responsible for this disease, designated XLRS1, was identified, and several deleterious gene mutations were reported.
Objective To analyze Japanese patients clinically diagnosed as having XLRS formutational changes in the XLRS1 gene.
Methods Ten patients with XLRS underwent full ophthalmologic examination, including slitlamp biomicroscopy and dilated funduscopy. Genomic DNA was isolated from leukocytes, and all exons of the XLRS1 gene were amplified by polymerase chain reaction and analyzed using a direct sequencing method.
Results Point mutations in the XLRS1 gene were identified in all 10 patients. The mutations were identical in each of 2 pairs of brothers. Six of the point mutations represented missense mutations, 1 was a nonsense mutation, and 1 was a frameshift mutation. Five of the mutations are newly reported herein.
Conclusions The discovery of new point mutations in this study increases the available information regarding the spectrum of genetic abnormalities and clinical manifestations of XLRS. However, the limited data failed to reveal a correlation between mutation and disease phenotype.
Clinical Relevance Identification of mutations in the XLRS1 gene and expanded information on clinical manifestations will facilitate early diagnosis, appropriate early therapy, and genetic counseling regarding the prognosis of XLRS.
From the Department of Ophthalmology and Visual Science, Osaka University Medical School, Osaka (Drs Y. Inoue, Yamamoto, M. Okada, Tsujikawa, T. Inoue, A. Okada, Kusaka, Saito, Fujikado, and Tano), Wakabayashi Eye Institute, Kanazawa (Dr Wakabayashi), and Department of Ophthalmology, Nagoya University Medical School, Nagoya (Dr Miyake), Japan.
 CiteULike  Connotea  Del.icio.us  Digg  Reddit  Technorati  Twitter
What's this?
THIS ARTICLE HAS BEEN CITED BY OTHER ARTICLES
Molecular modeling of retinoschisin with functional analysis of pathogenic mutations from human X-linked retinoschisis
Sergeev et al.
Hum Mol Genet 2010;:ddq006v2-ddq006.
ABSTRACT
| FULL TEXT
Correlation of Genetic and Clinical Findings in Spanish Patients with X-linked Juvenile Retinoschisis
Riveiro-Alvarez et al.
IOVS 2009;50:4342-4350.
ABSTRACT
| FULL TEXT
Vitreoretinal surgery without schisis cavity excision for the management of juvenile X linked retinoschisis
Garcia-Arumi et al.
Br J Ophthalmol 2008;92:1558-1560.
ABSTRACT
| FULL TEXT
Japanese X-linked Juvenile Retinoschisis: Conflict of Phenotype and Genotype With Novel Mutations in the XLRS1 Gene
Nakamura et al.
Arch Ophthalmol 2001;119:1553-1554.
FULL TEXT
|
