Cystic fibrosis mutation frequencies in an Irish population

Clin Genet. 2003 Feb;63(2):121-5. doi: 10.1034/j.1399-0004.2003.00017.x.

Abstract

The incidence of cystic fibrosis (CF) at birth in Ireland is 1/1461. Neonate CF genetic testing is not routinely performed in Ireland. Currently, screening is only carried out where there is clinical evidence or a family history to suggest disease. Here we report the frequencies of common CF mutations occurring in an Irish population composed of samples collected from western, mid-western and southern regions of Ireland. Rarer CF mutations were also identified in a selected number of CF patients. In addition, a number of polymorphisms were identified, some of which are reported to be functionally and phenotypically important.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cystic Fibrosis / epidemiology
  • Cystic Fibrosis / genetics*
  • Cystic Fibrosis Transmembrane Conductance Regulator / genetics*
  • DNA Mutational Analysis / methods
  • DNA Primers
  • Gene Frequency / genetics*
  • Humans
  • Ireland / epidemiology
  • Polymorphism, Genetic

Substances

  • CFTR protein, human
  • DNA Primers
  • Cystic Fibrosis Transmembrane Conductance Regulator