Analysis of the VSX1 gene in keratoconus patients from Saudi Arabia
نویسندگان
چکیده
PURPOSE To screen the visual system homebox 1 (VSX1) gene in Saudi Arabian keratoconus patients. METHODS We sequenced the entire coding region, exon-intron boundaries in clinically confirmed keratoconus patients (n=55) and 50 ethnically matched healthy controls. All cases and controls were unrelated. RESULTS Sequencing VSX1 revealed the presence of five nucleotide changes, 3 of which were non-coding (g.8326 G>A, g.10945 G>T, and g.11059 A>C) and 2 were synonymous-coding sequence changes (g.5053 G>T and g.8222 A>G). All five sequence changes were benign polymorphisms with no apparent clinical significance. CONCLUSIONS In our keratoconus cohort, no pathogenic VSX1 mutation(s) were identified.
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