Misdiagnosis of Huntington's disease
نویسندگان
چکیده
منابع مشابه
Huntingtin and the molecular pathogenesis of Huntingtons disease
Huntington’s disease (HD) is a late-onset neurodegenerative disorder that is caused by a CAG repeat expansion in the IT15 gene, which results in a long stretch of polyglutamine close to the amino-terminus of the HD protein huntingtin (htt). The normal function of htt, and the molecular mechanisms that contribute to the disease pathogenesis, are in the process of being elucidated. In this review...
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huntingtons disease (hd) is an autosomal dominant inherited disease characterized by involuntary movements, behavioral and personality changes, dementia and cognitive decline. although the mean age of onset is about 40 years, it varies from 5 to 79 years. therefore, at-risk individuals are never sure to have escaped the disease. hd is a member of the growing family of neurodegenerative disorder...
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ژورنال
عنوان ژورنال: The Lancet Psychiatry
سال: 2017
ISSN: 2215-0366
DOI: 10.1016/s2215-0366(16)30355-8