 |
 |

Clinical and Genetic Analysis of a Family Affected With Dominant Optic Atrophy (OPA1)
Jeremiah Brown, Jr, MD;
John H. Fingert;
Chris M. Taylor;
Max Lake, MD;
Val C. Sheffield, MD, PhD;
Edwin M. Stone, MD, PhD
Arch Ophthalmol. 1997;115(1):95-99.
Abstract
 |  |
Objectives To refine the dominant optic atrophy locus, OPA1, on chromosome 3q and to characterize the phenotype of a 6-generation family pedigree affected with this disease.
Methods Fifty-six family members had a complete eye examination. Clinical records of an additional 3 patients were reviewed. Goldmann perimetry and a 21-chip subtest of the Farnsworth-Munsell 100-Hue test were performed on selected patients. Affected patients, unaffected siblings, and potentially informative spouses were genotyped with short tandem repeat polymorphisms located on chromosome 3. The genotypic data were subjected to linkage analysis.
Results Thirty-four family members were found to be clinically affected. Most experienced vision loss (20/40 or poorer) in the first decade of life. Most (9 of the 16 eyes) progressed to 20/800 or poorer visual acuity by age 60 years, while 2 patients maintained visual acuities of 20/40 at that age. Affected patients had a 2- to 10-fold increase in the error score of a 21-chip subtest of the Farnsworth-Munsell 100-Hue test compared with age-matched unaffected family members. The optic nerve examination revealed temporal pallor and excavation in all affected individuals. Linkage analysis revealed significant lod scores with 9 markers. The highest lod score, 10.1 (u=0), was obtained with marker D3S2305. Analysis of recombinants narrowed the disease interval to approximately 3.8 centimorgans, flanked by D3S3669 (centromeric) and D3S1305 (telomeric).
Conclusions Most patients affected with dominant optic atrophy in this family progressed to legal blindness by middle age. Color vision testing is a sensitive method for detection of affected patients. The dominant optic atrophy locus, OPA1, has been refined by the identification of new flanking markers: D3S3669 (centromeric) and D3S1305 (telomeric).
Author Affiliations
From the Departments of Ophthalmology (Drs Brown and Stone and Mr Fingert and Ms Taylor) and Pediatrics (Dr Sheffield), The University of Iowa College of Medicine, Iowa City. Dr Lake is a private practitioner in Salina, Kan.
CiteULike Connotea Del.icio.us Digg Reddit Technorati Twitter
What's this?
THIS ARTICLE HAS BEEN CITED BY OTHER ARTICLES
 |
Reduction of Inner Retinal Thickness in Patients with Autosomal Dominant Optic Atrophy Associated with OPA1 Mutations
Ito et al.
IOVS 2007;48:4079-4086.
ABSTRACT
| FULL TEXT
The phenotype of normal tension glaucoma patients with and without OPA1 polymorphisms
Aung et al.
Br J Ophthalmol 2003;87:149-152.
ABSTRACT
| FULL TEXT
OPA1 mutations in patients with autosomal dominant optic atrophy and evidence for semi-dominant inheritance
Pesch et al.
Hum Mol Genet 2001;10:1359-1368.
ABSTRACT
| FULL TEXT
Spectrum, frequency and penetrance of OPA1 mutations in dominant optic atrophy
Toomes et al.
Hum Mol Genet 2001;10:1369-1378.
ABSTRACT
| FULL TEXT
Genetic Heterogeneity of Dominant Optic Atrophy, Kjer Type: Identification of a Second Locus on Chromosome 18q12.2-12.3
Kerrison et al.
Arch Ophthalmol 1999;117:805-810.
ABSTRACT
| FULL TEXT
Clinical and Functional Features of Patients With Dominant Optic Atrophy
Iannaccone and Votruba
Arch Ophthalmol 1999;117:287-288.
FULL TEXT
Clinical Features in Affected Individuals From 21 Pedigrees With Dominant Optic Atrophy
Votruba et al.
Arch Ophthalmol 1998;116:351-358.
ABSTRACT
| FULL TEXT
Genomic Mapping of Kjer Dominant Optic Atrophy
Wiggs
Arch Ophthalmol 1997;115:115-116.
ABSTRACT
|