Phenotypic features of Huntington's disease-like 2. |
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| Authors: | Ruth H Walker Joseph Jankovic Elizabeth O'Hearn Russell L Margolis |
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| Affiliation: | Department of Neurology, Veterans Affairs Medical Center, Bronx Mount Sinai School of Medicine, New York, New York 10029, USA. ruth.walker@mssm.edu |
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| 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. |
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| Keywords: | Huntington's disease‐like 2 chorea dystonia parkinsonism |
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