Identification of a novel 45 repeat unstable allele associated with a disease phenotype at the MJD1/SCA3 locus

Am J Med Genet B Neuropsychiatr Genet. 2005 Feb 5;133B(1):124-6. doi: 10.1002/ajmg.b.30088.

Abstract

We report a three generation Indian pedigree with the proband having 45 repeats at the Machado Joseph Disease (MJD)/spinocerebellar ataxia 3 (SCA3) disease locus. The proband exhibited clinical features of SCA and showed signs of cerebellar and brainstem atrophy on the MRI scan. The 45 repeat allele was unstable upon inter-generational transmission and was associated with a haplotype found in the majority of MJD/SCA3 patients from around the world. This is the smallest unstable allele reported till date at the MJD/SCA3 locus and may greatly reduce the gap between normal and pathological repeat ranges. This article contains supplementary material, which may be viewed at the American Journal of Medical Genetics website at http://www.interscience.wiley.com/jpages/0148-7299:1/suppmat/index.html.

Publication types

  • Case Reports
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aged
  • Alleles
  • Ataxin-3
  • Atrophy
  • Base Sequence
  • Brain Stem / pathology
  • Cerebellum / pathology
  • Family Health
  • Female
  • Haplotypes
  • Humans
  • India
  • Machado-Joseph Disease / genetics*
  • Machado-Joseph Disease / pathology
  • Magnetic Resonance Imaging
  • Male
  • Nerve Tissue Proteins / genetics*
  • Nuclear Proteins
  • Pedigree
  • Phenotype
  • Polymorphism, Single Nucleotide
  • Repressor Proteins
  • Trinucleotide Repeat Expansion / genetics
  • Trinucleotide Repeats / genetics*

Substances

  • Nerve Tissue Proteins
  • Nuclear Proteins
  • Repressor Proteins
  • ATXN3 protein, human
  • Ataxin-3