[Analysis of IDS gene mutation in a family affected with mucopolysaccharidosis typeⅡ]

Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2017 Feb 10;34(1):58-60. doi: 10.3760/cma.j.issn.1003-9406.2017.01.013.
[Article in Chinese]

Abstract

Objective: To detect potential mutation of iduronate-2-sulfatase (IDS) gene in a family affected with mucopolysaccharidosis type Ⅱ (MPS Ⅱ).

Methods: For the proband and his unaffected mother, the whole coding sequence of the IDS gene was analyzed with PCR and bidirectional Sanger sequencing.

Results: A novel splicing mutation, c.709-1G>A, was detected in the proband, for which his mother was heterozygous.

Conclusion: The c.709-1G>A splicing mutation of the IDS gene is probably causative for the MSP Ⅱ in the proband. Prenatal diagnosis for the mutation may avoid birth of further child affected with this disease.

Publication types

  • Case Reports

MeSH terms

  • Base Sequence
  • Child
  • DNA Mutational Analysis / methods
  • Family Health
  • Female
  • Genetic Predisposition to Disease / genetics*
  • Glycoproteins / genetics*
  • Glycoproteins / metabolism
  • Heterozygote
  • Humans
  • Iduronate Sulfatase / genetics*
  • Iduronate Sulfatase / metabolism
  • Male
  • Mothers
  • Mucopolysaccharidosis II / diagnosis
  • Mucopolysaccharidosis II / enzymology
  • Mucopolysaccharidosis II / genetics*
  • Mutation*

Substances

  • Glycoproteins
  • IDS protein, human
  • Iduronate Sulfatase