Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Case Reports
. 2003 Dec;18(12):1527-30.
doi: 10.1002/mds.10587.

Phenotypic features of Huntington's disease-like 2

Affiliations
Case Reports

Phenotypic features of Huntington's disease-like 2

Ruth H Walker et al. Mov Disord. 2003 Dec.

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.

PubMed Disclaimer

Publication types

LinkOut - more resources