Sorsby fundus dystrophy without a mutation in the TIMP-3 gene
- Jacqueline J M Assinka,b,
- Eric de Backerc,
- Jacoline B ten Brinka,
- Takeya Kohnoc,
- Paulus T V M de Jonga,b,d,
- Arthur A B Bergena,
- Francoise Meirec
- aDepartment Ophthalmogenetics, The Netherlands Ophthalmic Research Institute, Netherlands, bDepartment Epidemiology and Biostatistics, Erasmus University Rotterdam, Netherlands, cDepartment Ophthalmology, University Hospital of Ghent, Belgium, dDepartment Ophthalmology, Academic Medical Hospital, Amsterdam, Netherlands
- Francoise Meire, Department of Ophthalmology, University Hospital of Ghent, De Pintelaan 185, B 9000 Ghent, Belgium francoise.meire{at}rug.ac.be
- Accepted 14 January 2000
Abstract
AIMS To examine a large family with an autosomal dominant fundus dystrophy and to investigate whether or not mutations in TIMP-3 gene were involved.
METHODS A large family of 58 individuals with an autosomal dominant fundus dystrophy was examined ophthalmologically. A DNA linkage analysis in the 22q12.1-q13.2 region was performed. The TIMP-3 gene was screened for mutations in all five exons.
RESULTS In this large family 15 individuals were affected. All other individuals were found to be clinically unaffected. Pisciform flecks in the midperiphery and drusen-like deposits were the most typical ophthalmological finding in this family and were encountered from the fifth decade on. Chorioretinal atrophy and neovascularisation with disciform lesions characterised the disease from the sixth decade on. Linkage analysis using an affected only analysis, showed a maximum positive lod score of 3.94 at θ = 0.0 with marker D22S283. No mutations possibly causing Sorsby fundus dystrophy were found in either the exonic sequences, the promotor region, or the 3′UTR.
CONCLUSION The family in this pedigree has an autosomal dominant fundus dystrophy, which is most probably Sorsby fundus dystrophy. Although, in the linkage analysis, significant positive lod scores were found with the region 22q12.1-q13.2, no causative mutations could be identified in the TIMP-3 gene.
