Affiliation:
1. Federal University of Paraná, Brazil
Abstract
We describe seven patients with genetically confirmed Huntington's disease (HD) who had non-choreic movement disorders as presenting symptoms or signs. Patients with movement disorders other than chorea in the early stages tended to have larger CAG trinucleotide repeat expansion in comparison with more "typical" HD patients.
Subject
Neurology,Clinical Neurology
Cited by
16 articles.
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