Mutations of the iduronate-2-sulfatase (IDS) gene in patients with Hunter syndrome (mucopolysaccharidosis II)

Hum Mutat. 1994;4(2):128-31. doi: 10.1002/humu.1380040206.

Abstract

Genomic DNA and cDNA from fibroblasts from nine unrelated German patients with X-linked iduronate-2-sulfatase (IDS) deficiency showing variable clinical manifestation were screened for point mutations and small structural aberrations. Direct sequencing revealed a splice mutation skipping exon A, one nonsense mutation, and five missense mutations concerning the exons B, F and I of the IDS gene. Several novel missense mutations were found: A68E, S426X, I485R, Q293H, and D478G. One of the point mutations eliminating a recognition site for the restriction enzyme MspI was used as a direct marker for a prenatal diagnosis. A relationship between type of mutation and clinical picture could not be recognized.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Female
  • Humans
  • Iduronate Sulfatase / genetics*
  • Male
  • Mucopolysaccharidosis II / diagnosis
  • Mucopolysaccharidosis II / genetics*
  • Pedigree
  • Point Mutation*
  • Polymerase Chain Reaction
  • Pregnancy
  • Prenatal Diagnosis
  • Sequence Analysis, DNA

Substances

  • Iduronate Sulfatase