Phenotypic features of Huntington's disease-like 2

被引：46

作者：

Walker, RH

Jankovic, J

O'Hearn, E

Margolis, RL

机构：

[1] CUNY Mt Sinai Sch Med, Dept Neurol, New York, NY 10029 USA

[2] Johns Hopkins Univ, Sch Med, Program Cellular & Mol Med, Baltimore, MD USA

[3] Johns Hopkins Univ, Sch Med, Dept Psychiat, Baltimore, MD USA

[4] Johns Hopkins Univ, Sch Med, Dept Neurol & Neurosci, Baltimore, MD USA

[5] Baylor Coll Med, Dept Neurol, Houston, TX 77030 USA

[6] Baylor Coll Med, Parkinsons Dis Ctr, Houston, TX 77030 USA

[7] Baylor Coll Med, Movement Disorders Clin, Houston, TX 77030 USA

[8] Vet Affairs Med Ctr, Dept Neurol, Bronx, NY USA

来源：

MOVEMENT DISORDERS | 2003年 / 18卷 / 12期

关键词：

Huntington's disease-like 2; chorea; dystonia; parkinsonism;

D O I：

10.1002/mds.10587

中图分类号：

R74 [神经病学与精神病学];

学科分类号：

摘要：

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. (C) 2003 Movement Disorder Society.

引用

页码：1527 / 1530

页数：4

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