Screening for CRX gene mutations in Chinese patients with Leber congenital amaurosis and mutational phenotype

Ophthalmic Genet. 2001 Jun;22(2):89-96. doi: 10.1076/opge.22.2.89.2227.

Abstract

Purpose: To screen for possible disease-causing mutations in the CRX gene in Chinese patients with Leber congenital amaurosis (LCA) and to enrich the understanding of its mutational phenotype.

Methods: Genomic DNA was collected from 27 patients with LCA. The coding sequences of the CRX gene were analyzed using the PCR-heteroduplex-SSCP method. Mutations were confirmed by DNA sequencing.

Results: We identified two heterozygous variations in the CRX gene in two patients with LCA. One was a deletion (GCC-->-CC, A181D1bp) leading to a frameshift and protein truncation. This mutation was present in a patient with LCA, but not in his healthy parents. The ocular manifestations of this A181Delta1bp mutation are described. An intronic variation (IVS1-13G-->C) was found in a patient with LCA as well as in his healthy father.

Conclusion: A heterozygous A181D1bp mutation in the CRX gene caused an LCA phenotype in a Chinese patient.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Asian People
  • Blindness / ethnology
  • Blindness / genetics*
  • Blindness / pathology
  • China / epidemiology
  • DNA / analysis
  • DNA Mutational Analysis
  • Female
  • Fluorescein Angiography
  • Gene Frequency
  • Genetic Testing
  • Genotype
  • Homeodomain Proteins / genetics*
  • Humans
  • Male
  • Mutation*
  • Optic Atrophies, Hereditary / ethnology
  • Optic Atrophies, Hereditary / genetics*
  • Optic Atrophies, Hereditary / pathology
  • Pedigree
  • Phenotype
  • Polymerase Chain Reaction
  • Polymorphism, Single-Stranded Conformational
  • Trans-Activators / genetics*

Substances

  • Homeodomain Proteins
  • Trans-Activators
  • cone rod homeobox protein
  • DNA