Familial Amyotrophic Lateral Sclerosis

Neurol Clin. 2015 Nov;33(4):807-30. doi: 10.1016/j.ncl.2015.07.001. Epub 2015 Sep 8.

Abstract

Genes linked to amyotrophic lateral sclerosis (ALS) susceptibility are being identified at an increasing rate owing to advances in molecular genetic technology. Genetic mechanisms in ALS pathogenesis seem to exert major effects in about 10% of patients, but genetic factors at some level may be important components of disease risk in most patients with ALS. Identification of gene variants associated with ALS has informed concepts of the pathogenesis of ALS, aided the identification of therapeutic targets, facilitated research to develop new ALS biomarkers, and supported the establishment of clinical diagnostic tests for ALS-linked genes.

Keywords: ALS; Amyotrophic lateral sclerosis; Familial ALS; Genetic testing; Genetics; Phenotypes.

Publication types

  • Review

MeSH terms

  • Amyotrophic Lateral Sclerosis / genetics*
  • C9orf72 Protein
  • DNA-Binding Proteins / genetics
  • Family Health*
  • Genetic Predisposition to Disease / genetics*
  • Humans
  • Mutation / genetics*
  • Proteins / genetics
  • RNA-Binding Protein FUS / genetics
  • Superoxide Dismutase / genetics
  • Superoxide Dismutase-1

Substances

  • C9orf72 Protein
  • C9orf72 protein, human
  • DNA-Binding Proteins
  • FUS protein, human
  • Proteins
  • RNA-Binding Protein FUS
  • SOD1 protein, human
  • TARDBP protein, human
  • Superoxide Dismutase
  • Superoxide Dismutase-1