Frontotemporal demens heterogen sjukdomsgrupp.
(2009) In Läkartidningen 106(20). p.1381-1385- Abstract
- 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... (More)
- 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. (Less)
Please use this url to cite or link to this publication:
https://lup.lub.lu.se/record/1453267
- author
- Landqvist, Maria
LU
; Elfgren, Christina LU
; Englund, Elsabet ; Nilsson, Christer LU and Passant, Ulla LU
- organization
- publishing date
- 2009
- type
- Contribution to journal
- publication status
- published
- subject
- keywords
- Dementia: classification, Brain: pathology, Dementia: genetics, Dementia: diagnosis, Dementia: pathology
- in
- Läkartidningen
- volume
- 106
- issue
- 20
- pages
- 1381 - 1385
- publisher
- Swedish Medical Association
- external identifiers
-
- pmid:19585835
- scopus:67650115761
- ISSN
- 0023-7205
- language
- Swedish
- LU publication?
- yes
- additional info
- The information about affiliations in this record was updated in December 2015. The record was previously connected to the following departments: Department of Psychogeriatrics (013304000), Department of Psychology (012010000)
- id
- 8542ee4d-f8a7-4a08-a046-0aee8b9a163d (old id 1453267)
- alternative location
- http://www.ncbi.nlm.nih.gov/pubmed/19585835?dopt=Abstract
- http://ltarkiv.lakartidningen.se/artNo36567
- date added to LUP
- 2016-04-04 09:11:10
- date last changed
- 2024-10-12 22:30:01
@article{8542ee4d-f8a7-4a08-a046-0aee8b9a163d, abstract = {{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.}}, author = {{Landqvist, Maria and Elfgren, Christina and Englund, Elsabet and Nilsson, Christer and Passant, Ulla}}, issn = {{0023-7205}}, keywords = {{Dementia: classification; Brain: pathology; Dementia: genetics; Dementia: diagnosis; Dementia: pathology}}, language = {{swe}}, number = {{20}}, pages = {{1381--1385}}, publisher = {{Swedish Medical Association}}, series = {{Läkartidningen}}, title = {{Frontotemporal demens heterogen sjukdomsgrupp.}}, url = {{http://www.ncbi.nlm.nih.gov/pubmed/19585835?dopt=Abstract}}, volume = {{106}}, year = {{2009}}, }