High prevalence of a point mutation in the porphobilinogen deaminase gene in Dutch patients with acute intermittent porphyria

Hum Genet. 1993 Mar;91(2):128-30. doi: 10.1007/BF00222712.

Abstract

Acute intermittent porphyria (AIP) is an autosomal dominant disease characterized by a deficiency of porphobilinogen deaminase (PBGD). Up to now 14 different mutations have been described. In an effort to investigate the molecular epidemiology of AIP we have undertaken a systematic study of different exons of the PBGD gene from a large number of unrelated patients. Here, exon 8 from 82 unrelated Dutch and French AIP patients was examined using single strand confirmation polymorphism analysis (SSCP) after polymerase chain reaction (PCR) amplification. A single base mutation, C to T, at position 346 of the sequence coding for PBGD was observed in 15 Dutch families but in only 1 French family. A simple PCR assay is described to facilitate the diagnosis of this common mutation at the DNA level.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Base Sequence
  • DNA Mutational Analysis / methods*
  • DNA, Single-Stranded / analysis
  • France
  • Gene Frequency
  • Humans
  • Hydroxymethylbilane Synthase / genetics*
  • Molecular Sequence Data
  • Netherlands
  • Nucleic Acid Conformation
  • Point Mutation*
  • Polymerase Chain Reaction
  • Polymorphism, Restriction Fragment Length
  • Porphyria, Acute Intermittent / genetics*
  • Prevalence

Substances

  • DNA, Single-Stranded
  • Hydroxymethylbilane Synthase