Literature DB >> 20561037

Frontotemporal dementia and parkinsonism linked to chromosome 17--the first Polish family.

E Narożańska1, B Jasińska-Myga, E J Sitek, P Robowski, B Brockhuis, P Lass, M Dubaniewicz, D Wieczorek, M Baker, R Rademakers, Z K Wszolek, J Sławek.   

Abstract

BACKGROUND: Frontotemporal dementia and parkinsonism linked to chromosome 17 (FTDP-17) is a neurodegenerative disorder with various clinical phenotypes. We present the first Central-Eastern European family (Gdansk Family) with FTDP-17 because of a P301L mutation in microtubule-associated protein tau (MAPT).
METHODS: We have studied a family consisting of 82 family members, 39 of whom were genetically evaluated. The proband and her affected brother underwent detailed clinical and neuropsychological examinations.
RESULTS: P301L mutation in MAPT was identified in two affected and five asymptomatic family members. New features included hemispatial neglect and unilateral resting tremor not previously reported for P301L MAPT mutation. Low blood folic acid levels were also detected.
CONCLUSIONS: Our report suggests that FTDP-17 affects patients worldwide, but because of its heterogenous clinical presentation remains underrecognized.
© 2010 The Author(s). European Journal of Neurology © 2010 EFNS.

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Year:  2011        PMID: 20561037      PMCID: PMC2944014          DOI: 10.1111/j.1468-1331.2010.03107.x

Source DB:  PubMed          Journal:  Eur J Neurol        ISSN: 1351-5101            Impact factor:   6.089


  12 in total

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Review 3.  Frontotemporal dementia and parkinsonism linked to chromosome 17: a consensus conference. Conference Participants.

Authors:  N L Foster; K Wilhelmsen; A A Sima; M Z Jones; C J D'Amato; S Gilman
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4.  Unilateral neglect in a patient diagnosed with frontotemporal dementia and parkinsonism linked to chromosome 17.

Authors:  Emilia J Sitek; Ewa Narożańska; Jarosław Sławek; Dariusz Wieczorek; Bogna Brockhuis; Piotr Lass; Mirosława Dubaniewicz; Barbara Jasińska-Myga; Matt Baker; Rosa Rademakers; Zbigniew K Wszołek
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Review 6.  Phenotypic correlations in FTDP-17.

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  4 in total

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

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Review 2.  Characterization of Movement Disorder Phenomenology in Genetically Proven, Familial Frontotemporal Lobar Degeneration: A Systematic Review and Meta-Analysis.

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3.  Assessment of Olfactory Function in MAPT-Associated Neurodegenerative Disease Reveals Odor-Identification Irreproducibility as a Non-Disease-Specific, General Characteristic of Olfactory Dysfunction.

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4.  Creation of an open-access, mutation-defined fibroblast resource for neurological disease research.

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