D11Y SOD1 mutation and benign ALS: a consistent genotype-phenotype correlation

J Neurol Sci. 2011 Oct 15;309(1-2):31-3. doi: 10.1016/j.jns.2011.07.041. Epub 2011 Aug 11.

Abstract

We describe three sporadic ALS patients in which a D11Y SOD1 mutation was detected. All three patients disclosed a prolonged survival and a stereotypical distal limbs involvement in the initial stages of the disease. By this report we demonstrate that D11Y SOD1 mutation is associated with a peculiar phenotype and we confirm its probable pathogenetic role.

Publication types

  • Case Reports
  • Comparative Study

MeSH terms

  • Aged
  • Amino Acid Substitution / genetics
  • Amyotrophic Lateral Sclerosis / diagnosis*
  • Amyotrophic Lateral Sclerosis / genetics*
  • Aspartic Acid / genetics
  • Female
  • Genetic Association Studies* / methods
  • Humans
  • Middle Aged
  • Mutation / genetics*
  • Superoxide Dismutase / genetics*
  • Superoxide Dismutase-1
  • Tyrosine / genetics

Substances

  • SOD1 protein, human
  • Aspartic Acid
  • Tyrosine
  • Superoxide Dismutase
  • Superoxide Dismutase-1