The mutation delta F508 on Dutch cystic fibrosis chromosomes: frequency and relation to patients age at diagnosis

Hum Genet. 1990 Sep;85(4):407-8. doi: 10.1007/BF02428281.

Abstract

We tested 190 chromosomes from Dutch cystic fibrosis (CF) patients and carriers for the presence or absence of the major CF mutation delta F508. This mutation was found on 77% of the Dutch CF chromosomes. We observed a significant difference in the distribution of the ages at diagnosis between homozygotes for delta F508 and the other patients. delta F508 homozygotes tend to be identified as patients at neonatal or infantile age. The age at diagnosis of patients with at least one unknown allele, on the other hand, ranged between neonatal and young adult age.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Adult
  • Age Factors
  • Child
  • Child, Preschool
  • Chromosome Deletion
  • Cystic Fibrosis / epidemiology
  • Cystic Fibrosis / genetics*
  • Gene Frequency
  • Heterozygote
  • Humans
  • Infant
  • Infant, Newborn
  • Netherlands / epidemiology