Literature DB >> 23121543

Agraphia in patients with frontotemporal dementia and parkinsonism linked to chromosome 17 with P301L MAPT mutation: dysexecutive, aphasic, apraxic or spatial phenomenon?

Emilia J Sitek1, Ewa Narozanska, Anna Barczak, Barbara Jasinska-Myga, Michał Harciarek, Małgorzata Chodakowska-Zebrowska, Małgorzata Kubiak, Dariusz Wieczorek, Seweryna Konieczna, Rosa Rademakers, Matt Baker, Mariusz Berdynski, Bogna Brockhuis, Maria Barcikowska, Cezary Zekanowski, Kenneth M Heilman, Zbigniew K Wszolek, Jarosław Slawek.   

Abstract

OBJECTIVES: Patients with frontotemporal dementia and parkinsonism linked to chromosome 17 (FTDP-17) may be agraphic. The study aimed at characterizing agraphia in individuals with a P301L MAPT mutation.
METHODS: Two pairs of siblings with FTDP-17 were longitudinally examined for agraphia in relation to language and cognitive deficits.
RESULTS: All patients presented with dysexecutive agraphia. In addition, in the first pair of siblings one sibling demonstrated spatial agraphia with less pronounced allographic agraphia and the other sibling had aphasic agraphia. Aphasic agraphia was also present in one sibling from the second pair.
CONCLUSION: Agraphia associated with FTDP-17 is very heterogeneous.

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Year:  2012        PMID: 23121543      PMCID: PMC3710298          DOI: 10.1080/13554794.2012.732087

Source DB:  PubMed          Journal:  Neurocase        ISSN: 1355-4794            Impact factor:   0.881


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