A novel 22bp deletion in a Tunisian phenylketonuria family

Pathol Biol (Paris). 2012 Dec;60(6):e87-9. doi: 10.1016/j.patbio.2012.03.007. Epub 2012 May 7.

Abstract

Phenylketonuria (PKU) is an autosomal recessive metabolic disorder caused by a deficiency of phenylalanine hydroxylase. To date, more than 530 mutations in the PAH gene have been reported. In Tunisia, this disease seems to be the result of point mutations, few studies have been published about molecular defects of PKU in our country. In this study, we report a novel deletion in exon 6 of two brothers in a Tunisian family after DHPLC analysis and sequencing of the exon 6 of the PAH gene.

Publication types

  • Case Reports

MeSH terms

  • Base Sequence
  • Child, Preschool
  • Consanguinity
  • Exons
  • Humans
  • Male
  • Mutation
  • Phenylalanine Hydroxylase / genetics
  • Phenylketonurias / genetics*
  • Sequence Deletion / genetics*
  • Tunisia

Substances

  • Phenylalanine Hydroxylase