Parental origin of mutations in sporadic cases of Treacher Collins syndrome

Eur J Hum Genet. 2003 Sep;11(9):718-22. doi: 10.1038/sj.ejhg.5201029.

Abstract

In some autosomal dominant conditions, there is a correlation between new mutations and paternal age, with new mutations arising almost exclusively in the male germ line. To test this hypothesis in Treacher Collins syndrome, we analyzed 22 sporadic cases, determining the parental origin of the pathogenic mutation in 10 informative families. Mutations were found to be of both paternal and maternal origin, without a detectable parental age effect, confirming that a paternal age effect is not universal to all autosomal dominant disorders. A discussion on the parental origin of mutations and paternal age effect in other diseases is included.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Electrophoresis
  • Genes, Dominant / genetics*
  • Genetic Markers
  • Humans
  • Mandibulofacial Dysostosis / genetics*
  • Mutation / genetics*
  • Nuclear Proteins / genetics*
  • Parents
  • Pedigree
  • Phosphoproteins / genetics*
  • Polymorphism, Single Nucleotide
  • Polymorphism, Single-Stranded Conformational
  • Sequence Analysis, DNA

Substances

  • Genetic Markers
  • Nuclear Proteins
  • Phosphoproteins
  • TCOF1 protein, human