Exome analysis reveals a Japanese family with spinocerebellar ataxia, autosomal recessive 1

J Neurol Sci. 2013 Aug 15;331(1-2):158-60. doi: 10.1016/j.jns.2013.05.018. Epub 2013 Jun 18.

Abstract

Spinocerebellar ataxia autosomal recessive 1 (SCAR1/AOA2) is clinically characterized by an early-onset progressive cerebellar ataxia with axonal neuropathy, ocular motor apraxia, and elevation of serum alpha-fetoprotein level. The disorder is caused by mutations in senataxin (SETX) gene. Here, we report a Japanese SCAR1/AOA2 family with a homozygous nonsense mutation (p.Q1441X) of SETX that was identified by exome sequencing. The family was previously reported as early-onset ataxia of undetermined cause. The present study emphasized the role of whole exome-sequence analysis to establish the molecular diagnosis of neurodegenerative disease presenting with diverse clinical presentations.

Keywords: Alpha-fetoprotein; Autosomal recessive 1; Exome analysis; Exon capture; Linkage analysis; Massively parallel sequencing; SETX; Spinocerebellar ataxia.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • DNA Helicases
  • DNA Mutational Analysis
  • Exome / genetics*
  • Family Health*
  • Female
  • Genetic Linkage
  • Humans
  • Japan
  • Male
  • Multifunctional Enzymes
  • Polymorphism, Single Nucleotide / genetics*
  • RNA Helicases / genetics*
  • Spinocerebellar Ataxias / congenital
  • Spinocerebellar Degenerations / genetics*

Substances

  • Multifunctional Enzymes
  • SETX protein, human
  • DNA Helicases
  • RNA Helicases

Supplementary concepts

  • Spinocerebellar ataxia, autosomal recessive 1