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Progressive supranuclear palsy in a family with TDP-43 pathology
A Kertesz1, E Finger, J Murrell
1a Department of Clinical Neurological Sciences , Schulich School of Medicine and Dentistry, University of Western Ontario , 39 Doncaster Ave, London , ON , N6G 2A1 , Canada.
Unlabelled:
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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