Variable phenotypic expressivity in a Swiss family with autosomal dominant retinitis pigmentosa due to a T494M mutation in the PRPF3 gene.


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Variable phenotypic expressivity in a Swiss family with autosomal dominant retinitis pigmentosa due to a T494M mutation in the PRPF3 gene.
Molecular Vision
Vaclavik V., Gaillard M.C., Tiab L., Schorderet D.F., Munier F.L.
1090-0535[electronic], 1090-0535[linking]
Statut éditorial
Date de publication
Publication types: Journal Article ; Research Support, Non-U.S. Gov't
Publication Status: epublish
PURPOSE: To characterize the clinical, psychophysical, and electrophysiological phenotypes in a five-generation Swiss family with dominantly inherited retinitis pigmentosa caused by a T494M mutation in the Precursor mRNA-Processing factor 3 (PRPF3) gene, and to relate the phenotype to the underlying genetic mutation. METHODS: Eleven affected patients were ascertained for phenotypic and genotypic characterization. Ophthalmologic evaluations included color vision testing, Goldmann perimetry, and digital fundus photography. Some patients had autofluorescence imaging, Optical Coherence Tomography, and ISCEV-standard full-field electroretinography. All affected patients had genetic testing. RESULTS: The age of onset of night blindness and the severity of the progression of the disease varied between members of the family. Some patients reported early onset of night blindness at age three, with subsequent severe deterioration of visual acuity, which was 0.4 in the best eye after their fifties. The second group of patients had a later onset of night blindness, in the mid-twenties, with a milder disease progression and a visual acuity of 0.8 at age 70. Fundus autofluorescence imaging and electrophysiological and visual field abnormalities also showed some degree of varying phenotypes. The autofluorescence imaging showed a large high-density ring bilaterally. Myopia (range: -0.75 to -8) was found in 10/11 affected subjects. Fundus findings showed areas of atrophy along the arcades. A T494M change was found in exon 11 of the PRPF3 gene. The change segregates with the disease in the family. CONCLUSIONS: A mutation in the PRPF3 gene is rare compared to other genes causing autosomal dominant retinitis pigmentosa (ADRP). Although a T494M change has been reported, the family in our study is the first with variable expressivity. Mutations in the PRPF3 gene can cause a variable ADRP phenotype, unlike in the previously described Danish, English, and Japanese families. Our report, based on one of the largest affected pedigree, provides a better understanding as to the phenotype/genotype description of ADRP caused by a PRPF3 mutation.
Adult, Aged, Amino Acid Substitution/genetics, Base Sequence, Child, Child, Preschool, DNA Mutational Analysis, Electroretinography, Family, Female, Fluorescence, Fundus Oculi, Genes, Dominant/genetics, Humans, Male, Methionine/genetics, Middle Aged, Molecular Sequence Data, Mutation/genetics, Nuclear Proteins/genetics, Phenotype, Retinitis Pigmentosa/genetics, Ribonucleoprotein, U4-U6 Small Nuclear/genetics, Switzerland, Threonine/genetics, Young Adult
Web of science
Création de la notice
18/05/2010 12:56
Dernière modification de la notice
20/08/2019 14:39
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