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Clinical Features and Neuropathology of Autosomal Dominant Spinocerebellar Ataxia (SCA17) Ann Neurol 43:367-375, Rolfs,A.,et al, 2003 See this aricle in Pubmed Article Abstract Based on clinical and genetic data, we conclude that SCA17 is rare among white SCA patients. SCA17 should be considered in sporadic and familial cases of ataxia with accompanying psychiatric symptoms and dementia.

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(click to filter results - removes previous filter) ataxia ataxia,hereditary dementia familial neuropathology psychiatric problems in neurologic disorders spinocerebellar ataxia spinocerebellar ataxia type 17 trinucleotide repeats

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