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Title
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Progressive Supranuclear Palsy in a family with TDP-43 pathology
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Author
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Abstract
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| A member of a family with an autosomal dominant pattern of frontotemporal dementia (FTD) with a TDP-43 pathological substrate in other members and no mutations in FTD-associated genes developed behavioral variant FTD followed by Progressive Supranuclear Palsy. Autopsy revealed a pure tauopathy of PSP pattern. Conclusions: The findings raise the possibility of shared pathogenic pathways and a proximal genetic abnormality between PSP and FTLD-43. |
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Language
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English
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Source (journal)
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Neurocase. - Oxford, 1997, currens
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Publication
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Oxford
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2015
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ISSN
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1355-4794
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DOI
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10.1080/13554794.2013.878729
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Volume/pages
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21
:2
(2015)
, p. 178-184
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ISI
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000346850300007
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Full text (Publisher's DOI)
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