Autopsy-proven Huntington's disease with 29 trinucleotide repeats

Christopher Kenney, Suzanne Zein-Eldin Powell, Joseph Jankovic

Research output: Contribution to journalArticlepeer-review

75 Scopus citations


Huntington's disease (HD) is a neurodegenerative disorder associated with expansion of CAG trinucleotide repeats in the huntingtin gene. A minimum of 36 CAG repeats is usually reported in patients with clinical features of HD; 30 to 35 repeats represent an intermediate range. Here we report a 65-year-old male with autopsy-proven HD and 29 CAG repeats.

Original languageEnglish (US)
Pages (from-to)127-130
Number of pages4
JournalMovement Disorders
Issue number1
StatePublished - Jan 2007


  • Autopsy
  • Chorea
  • Huntington's disease
  • Neuropathology
  • Phenocopy
  • Trinucleotide repeat

ASJC Scopus subject areas

  • Clinical Neurology
  • Neuroscience(all)


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