American journal of ophthalmology · 2006
Screening genes of the retinoid metabolism: novel LRAT mutation in leber congenital amaurosis.
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Sénéchal Audrey, Humbert Ghyslaine, Surget Marie-Odile, Bazalgette Cécile, Bazalgette Christian, Arnaud Bernard, Arndt Carl, Laurent Eric, Brabet Philippe, Hamel Christian P
Аннотация
PURPOSE: To evaluate the mutation prevalence and phenotype in genes involved in the ocular retinoid metabolism.
DESIGN: We analyzed LRAT, encoding the lecithin retinol acyltransferase, and RDH10, a retinal pigment epithelium-specific retinol dehydrogenase.
METHODS: We screened by denaturing-high performance liquid chromatography (D-HPLC) and direct sequencing all coding exons of LRAT and RDH10 in 216 patients, including 134 with simplex or multiplex retinitis pigmentosa and 82 with various types of flecked retinal dystrophies.
RESULTS: Only nonpathogenic variants were found in this series. In an additional 2.5-year-old patient presenting with an "RPE65" phenotype (night blindness, photoattractivity, and visual improvement several months after birth), we discovered a homozygous deletion in LRAT (c.217_218delAT) leading to a premature stop at codon 120.
CONCLUSIONS: The phenotype of patients with mutations in LRAT is similar to that of patients with mutations in RPE65, suggesting the need to systematically screen both genes in case of typical phenotype.
DESIGN: We analyzed LRAT, encoding the lecithin retinol acyltransferase, and RDH10, a retinal pigment epithelium-specific retinol dehydrogenase.
METHODS: We screened by denaturing-high performance liquid chromatography (D-HPLC) and direct sequencing all coding exons of LRAT and RDH10 in 216 patients, including 134 with simplex or multiplex retinitis pigmentosa and 82 with various types of flecked retinal dystrophies.
RESULTS: Only nonpathogenic variants were found in this series. In an additional 2.5-year-old patient presenting with an "RPE65" phenotype (night blindness, photoattractivity, and visual improvement several months after birth), we discovered a homozygous deletion in LRAT (c.217_218delAT) leading to a premature stop at codon 120.
CONCLUSIONS: The phenotype of patients with mutations in LRAT is similar to that of patients with mutations in RPE65, suggesting the need to systematically screen both genes in case of typical phenotype.
Предметные рубрики MeSH
AcyltransferasesAlcohol OxidoreductasesBlindnessCarrier ProteinsChild, PreschoolChromatography, High Pressure LiquidConsanguinityDNA Mutational AnalysisExonsEye ProteinsFrameshift MutationGenetic TestingHumansMalePedigreePhenotypePolymerase Chain ReactionRetinitis PigmentosaRetinoidsSequence Analysis, DNAcis-trans-IsomerasesRetinoid Isomerohydrolase