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- W2057631378 abstract "Chorea Huntington (CH) is a dominantly inherited, neurodegenerative disease usually with adult onset. The course of CH is characterized by movement disturbances, psychiatric symptoms and it may lead to dementia. Typically death occurs after 10 to 20 years of CH duration. Invariably, the underlying mutation concerns an expansion of a polymorphic (CAG) n stretch in the huntingtin gene. Statistically, larger expansions lead to earlier onset of the disease. We report on a girl with a huntingtin allele of > 140 (CAG) n repeats. Unspecific neurological symptoms were noted at the age of 4.3 years followed by rapid disease progression with psychomotor deterioration." @default.
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- W2057631378 date "2002-04-01" @default.
- W2057631378 modified "2023-09-24" @default.
- W2057631378 title "Chorea Huntington: A Rare Case with Childhood Onset" @default.
- W2057631378 doi "https://doi.org/10.1055/s-2002-32367" @default.
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