[Hereditary hemorrhagic telangiectasia resulted from a nonsense mutation Arg479 Stop in the ALK-1 gene]

Zhonghua Xue Ye Xue Za Zhi. 2004 Sep;25(9):536-9.
[Article in Chinese]

Abstract

Objective: To identify the gene mutations in a pedigree with hereditary hemorrhagic telangiectasia.

Methods: Genomic DNA was extracted from the peripheral blood of the propositus. All of the exons, intron/exon boundaries and the 5' untranslation regions (UTR) of the ALK-1 and endoglin gene were amplified by polymerase chain reaction (PCR). The PCR products were screened by direct sequencing.

Results: The mutation is a C1437T substitution in exon 10 of the ALK-1 gene, resulting in Arg 479 Stop.

Conclusion: The hereditary hemorrhagic telangiectasia propositus is caused by a heterozygous Arg 479 Stop mutation in the ALK-1 gene which has not been identified previously.

Publication types

  • Case Reports
  • English Abstract

MeSH terms

  • Activin Receptors, Type II / genetics*
  • Aged
  • Antigens, CD / genetics
  • Base Sequence
  • Codon, Nonsense*
  • DNA Mutational Analysis
  • Exons / genetics
  • Female
  • Humans
  • Male
  • Pedigree
  • Point Mutation
  • Receptors, Cell Surface / genetics
  • Telangiectasia, Hereditary Hemorrhagic / genetics*
  • Telangiectasia, Hereditary Hemorrhagic / pathology

Substances

  • Antigens, CD
  • Codon, Nonsense
  • Receptors, Cell Surface
  • Activin Receptors, Type II