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)
Cited by
26 articles.
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