Normal CAG repeat length in the Huntington's disease gene in senile chorea

Author:

Shinotoh Hitoshi,Calne Donald B.,Snow Barry,Hayward Margo,Kremer Berry,Theilmann Jane,Hayden Michael R.

Abstract

There is a widely held belief that most patients presenting with senile chorea have late-onset Huntington's disease (HD) with an unknown family history. We measured CAG trinucleotide repeat expansion in the HD gene in four patients with a clinical presentation of senile chorea and found that CAG repetition lengths were normal. These findings support senile chorea as being a distinct clinical entity that is nosologically separate from late-onset HD.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Neurology (clinical)

Cited by 26 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

1. Reply: Late onset Huntington's disease with 29 CAG repeat expansion;Journal of the Neurological Sciences;2016-09

2. Non-Parkinsonian Movement Disorders;Pathy's Principles and Practice of Geriatric Medicine;2012-03-12

3. Huntington Disease and Other Choreas;Hyperkinetic Movement Disorders;2012

4. Senile Chorea;Encyclopedia of Movement Disorders;2010

5. Chorea associated with gabapentin use in an elderly man;The American Journal of Geriatric Pharmacotherapy;2009-08

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