Phenotypic features of Huntington's disease-like 2

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

doi:10.1002/mds.10587

Phenotypic features of Huntington's disease-like 2

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

School of Medicine

Research output: Contribution to journal › Article › peer-review

53 Scopus citations

Abstract

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 language	English (US)
Pages (from-to)	1527-1530
Number of pages	4
Journal	Movement Disorders
Volume	18
Issue number	12
DOIs	https://doi.org/10.1002/mds.10587
State	Published - Dec 2003

Keywords

Chorea
Dystonia
Huntington's disease-like 2
Parkinsonism

ASJC Scopus subject areas

Neurology
Clinical Neurology

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10.1002/mds.10587

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abstract = "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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Phenotypic features of Huntington's disease-like 2

Abstract

Keywords

ASJC Scopus subject areas

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