Phenotypic features of Huntington's disease-like 2

Ruth H. Walker, Joseph Jankovic, Elizabeth O'Hearn, Russell L. Margolis

Research output: Contribution to journalArticlepeer-review

53 Scopus citations


Huntington's disease-like 2 is an autosomal dominantly inherited disorder due to an expansion of trinucleotide repeats. It resembles classic Huntington's disease in clinical phenotype, inheritance pattern, and neuropathological features. We highlight the clinical features of this disorder, including chorea, dystonia, parkinsonism, and cognitive deficits.

Original languageEnglish (US)
Pages (from-to)1527-1530
Number of pages4
JournalMovement Disorders
Issue number12
StatePublished - Dec 1 2003


  • Chorea
  • Dystonia
  • Huntington's disease-like 2
  • Parkinsonism

ASJC Scopus subject areas

  • Neurology
  • Clinical Neurology


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