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Article

Phenotypic features of Huntington's disease-like 2.

Movement disorders : official journal of the Movement Disorder Society - 1 Dec 2003

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

Abstract excerpt

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.

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Identifiers

PMID: 14673892
DOI: 10.1002/mds.10587

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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