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M. Gajecka, J. S. Wampole, L. B. Wallis, K. A. Bailey, A. Molinari, J. A. Pitarque, B. A. Bejjani; Gene Screening at the 13q32 Keratoconus Locus. Invest. Ophthalmol. Vis. Sci. 2009;50(13):4130.
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© ARVO (1962-2015); The Authors (2016-present)
Keratoconus (KTCN) is a non-inflammatory thinning and anterior protrusion of the cornea that results in steepening and distortion of the cornea, altered refractive powers, and altered visual acuity. We ascertained eighteen autosomal dominant multigenerational KTCN families from Ecuador and identified a novel locus on 13q32.1-q32.3. Here we present sequencing results of candidate keratoconus genes localized to 13q32.
Sixteen of the genes were chosen for the evaluation. Genes are screened by standard techniques using genomic DNA samples from all individuals from family KTCN-014 and selected affected and unaffected individuals from other Ecuadorian families. Coding exons and intron-exon boundaries of the genes are evaluated.
Sequencing analysis of genes MBNL2, FARP1, ZIC5, ZIC2, FGF14, EFNB2, RNF113B, DOCK9, PHGDHL1, VGCNL1, ERCG5 and ING1 have not revealed mutations segregated with the disease phenotype. Several novel single nucleotide polymorphisms were identified. Other candidate genes on 13q32.1-q32.3 are currently being screened for a possible role in the pathogenesis of KTCN.
To date, mutation analyses of candidate genes have not identified sequence alterations segregating with the keratoconus phenotype in this population.
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