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Title: Phenotypic features of Huntington's disease-like 2. Author: Walker RH, Jankovic J, O'Hearn E, Margolis RL. Journal: Mov Disord; 2003 Dec; 18(12):1527-30. PubMed ID: 14673892. 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.[Abstract] [Full Text] [Related] [New Search]