| Literature DB >> 17665004 |
Nilson Becker1, Renato P Munhoz, Salmo Raskin, Lineu César Werneck, Hélio A G Teive.
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.Entities:
Mesh:
Year: 2007 PMID: 17665004 DOI: 10.1590/s0004-282x2007000300007
Source DB: PubMed Journal: Arq Neuropsiquiatr ISSN: 0004-282X Impact factor: 1.420