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Författare: Landqvist Maria, Elfgren Christina, Englund Elisabet, Nilsson Christer, Passant Ulla

Titel: Frontotemporal demens heterogen sjukdomsgrupp [summary] (serie: Tema demens) 2009 nr 20 sid 1381-5

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Summary:
Frontotemporal lobar degeneration (FTLD) or frontotemporal dementia (FTD) is a clinically and neuropathologically heterogeneous group of primary degenerative dementia diseases. The clinical representation consists of progressive psychiatric and/or neurological symtoms such as behavioural changes, language or motor dysfunction. FTD is usually divided into the following subgroups: Behavioural variant FTD (FTD-bv), semantic dementia (SD), progressive non-fluent aphasia (PNFA) and FTD with motor neuron disease (FTD-MND). Progressive supranuclear palsy (PSP) and corticobasal degeneration (CBD) show both clinical and neuropathological similarities to FTD, and therefore are often considered being part of the FTD complex. Knowledge about the great diversity in phenotype of FTD facilitates early refererral and diagnosis of patients, which is necessary for adequate support and treatment.

Maria Landqvist, Christina Elfgren, Elisabet Englund, Christer Nilsson, Ulla Passant

Correspondence: Maria Landqvist, Avdelningen för geriatrisk psykiatri, Verksamhetsområde Kognitiv medicin, Universitetssjukhuset, SE-221 85 Lund, Sweden
maria.landqvist@med.lu.se

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Format för användning i referenslista:
Landqvist M, Elfgren C, Englund E, Nilsson C, Passant U. Frontotemporal demens heterogen sjukdomsgrupp. Läkartidningen 2009;106:1381-5.