We found a match
Your institution may have rights to this item. Sign in to continue.
- Title
Phenotypic features of Huntington's disease-like 2 (A videotape accompanies this article.).
- Authors
Ruth H. Walker; Joseph Jankovic; Elizabeth O'Hearn; Russell L. Margolis
- Abstract
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. © 2003 Movement Disorder Society
- Subjects
HUNTINGTON disease; GENETIC disorders; NEUROLOGIC manifestations of general diseases; MEDICAL genetics; PARKINSON'S disease; DYSTONIA
- Publication
Movement Disorders, 2003, Vol 18, Issue 12, p1527
- ISSN
0885-3185
- Publication type
Article
- DOI
10.1002/mds.10587