Article
Clinical expression of X-linked retinitis pigmentosa in a Swedish family with the RP2 genotype.
Ophthalmic genetics - 1 Dec 1998
Ponjavic V, Andréasson S, Abrahamson M, Ehinger B, Gieser L, Fujita R, Swaroop A
Abstract excerpt
PURPOSE: To examine the clinical phenotype with emphasis on electroretinograms and visual fields in a Swedish family with X-linked retinitis pigmentosa (XLRP) type 2 (RP2), and compare it with Swedish XLRP families with the RP3 genotype. METHODS: Three affected brothers and their carrier mother w...
Topics
- Adolescent
- Adult
- Cataract
- Dark Adaptation
- Electroretinography
- Female
- Genetic Linkage
- Genotype
- Humans
- Male
- Middle Aged
- Pedigree
- Refraction, Ocular
- Retinitis Pigmentosa
- Sensory Thresholds
- Sweden
- Visual Acuity
- Visual Fields