[Molecular screening of the major mutations in the ARSA gene in patients with metachromatic leukodystrophy]

Tsitol Genet. 2002 Sep-Oct;36(5):43-8.
[Article in Ukrainian]

Abstract

Metachromatic leukodystrophy (MLD) is an inherited storage disease caused by deficiency of arylsulfatase A (ARSA). Molecular analysis of the major mutations in the ARSA gene was performed in 10 Ukrainian patients (from 9 families) with MLD. According to the age of onset, late infantile MLD was identified in 3 patients, juvenile MLD in 5 patients, and adult MLD in 2 patients (sibs), respectively. The ARSA activity in the patients was 2-26 nmol/h/mg protein (the normal activity has been established in our laboratory as 111.9 +/- 7.1 nmol/h/mg protein). No correlation between enzyme activity and a clinical course of disease was revealed. The IVS2 + 1 mutation was found at 2 of 20 alleles (in a patient with late infantile form) and the P426L mutation was found at 2 of 20 alleles (in two patients with juvenile form). Thus, the total frequency of these two major mutations in the ARSA gene is 20% in Ukrainian MLD patients.

Publication types

  • English Abstract

MeSH terms

  • Alleles
  • Cerebroside-Sulfatase / genetics*
  • Cerebroside-Sulfatase / metabolism
  • DNA Primers / genetics
  • Female
  • Gene Frequency
  • Humans
  • Leukodystrophy, Metachromatic / enzymology
  • Leukodystrophy, Metachromatic / genetics*
  • Male
  • Mutation*
  • Polymorphism, Restriction Fragment Length

Substances

  • DNA Primers
  • Cerebroside-Sulfatase