Frontotemporal dementia.

Detalhes bibliográficos
Autor(a) principal: Guimarães, Joana
Data de Publicação: 2007
Outros Autores: Fonseca, Rosália, Garrett, Carolina
Tipo de documento: Artigo
Idioma: por
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: https://www.actamedicaportuguesa.com/revista/index.php/amp/article/view/963
Resumo: Frontotemporal dementia (FTD), although less common than Alzheimer's, constitutes a significant percentage of the degenerative dementias, making up 8 to 17% of patients who die with dementia before the age of 70. Several clinical presentations have been described for many authors, which are included in classical behaviour disorder of frontal lobe dementia and in language alterations of progressive aphasias. Classification and diagnosis criteria's of FTP are sometime controversial in literature. So, the authors give an overview of principal's aspects in this area, with focus on clinical, imagiological, patghological and genetic perspective. Furthermore, taken in account this revision was also made a characterization of the patients followed in Dementia Outpatient Clinical Care of our hospital. In these patient characteristics review the follow parameters were analysed: FDT clinical diagnosis; demographics, clinical, imagiological, neuropsychological aspects; and disease evolution. An retrospective study that allowed correlation between some aspects, namely clinical presentation with imagiological and neuropsychological findings. With this revision work, the authors pretend to alert for the relevance of FTD diagnosis, probably misdiagnosticated.
id RCAP_823fb0f14b5a430c86bbd5395ecc80d0
oai_identifier_str oai:ojs.www.actamedicaportuguesa.com:article/963
network_acronym_str RCAP
network_name_str Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
repository_id_str 7160
spelling Frontotemporal dementia.Demência frontotemporal: que entidade?Frontotemporal dementia (FTD), although less common than Alzheimer's, constitutes a significant percentage of the degenerative dementias, making up 8 to 17% of patients who die with dementia before the age of 70. Several clinical presentations have been described for many authors, which are included in classical behaviour disorder of frontal lobe dementia and in language alterations of progressive aphasias. Classification and diagnosis criteria's of FTP are sometime controversial in literature. So, the authors give an overview of principal's aspects in this area, with focus on clinical, imagiological, patghological and genetic perspective. Furthermore, taken in account this revision was also made a characterization of the patients followed in Dementia Outpatient Clinical Care of our hospital. In these patient characteristics review the follow parameters were analysed: FDT clinical diagnosis; demographics, clinical, imagiological, neuropsychological aspects; and disease evolution. An retrospective study that allowed correlation between some aspects, namely clinical presentation with imagiological and neuropsychological findings. With this revision work, the authors pretend to alert for the relevance of FTD diagnosis, probably misdiagnosticated.Frontotemporal dementia (FTD), although less common than Alzheimer's, constitutes a significant percentage of the degenerative dementias, making up 8 to 17% of patients who die with dementia before the age of 70. Several clinical presentations have been described for many authors, which are included in classical behaviour disorder of frontal lobe dementia and in language alterations of progressive aphasias. Classification and diagnosis criteria's of FTP are sometime controversial in literature. So, the authors give an overview of principal's aspects in this area, with focus on clinical, imagiological, patghological and genetic perspective. Furthermore, taken in account this revision was also made a characterization of the patients followed in Dementia Outpatient Clinical Care of our hospital. In these patient characteristics review the follow parameters were analysed: FDT clinical diagnosis; demographics, clinical, imagiological, neuropsychological aspects; and disease evolution. An retrospective study that allowed correlation between some aspects, namely clinical presentation with imagiological and neuropsychological findings. With this revision work, the authors pretend to alert for the relevance of FTD diagnosis, probably misdiagnosticated.Ordem dos Médicos2007-01-23info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttps://www.actamedicaportuguesa.com/revista/index.php/amp/article/view/963oai:ojs.www.actamedicaportuguesa.com:article/963Acta Médica Portuguesa; Vol. 19 No. 4 (2006): July-August; 319-24Acta Médica Portuguesa; Vol. 19 N.º 4 (2006): Julho-Agosto; 319-241646-07580870-399Xreponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAPporhttps://www.actamedicaportuguesa.com/revista/index.php/amp/article/view/963https://www.actamedicaportuguesa.com/revista/index.php/amp/article/view/963/636Guimarães, JoanaFonseca, RosáliaGarrett, Carolinainfo:eu-repo/semantics/openAccess2022-12-20T10:57:14Zoai:ojs.www.actamedicaportuguesa.com:article/963Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T16:16:52.920873Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãofalse
dc.title.none.fl_str_mv Frontotemporal dementia.
Demência frontotemporal: que entidade?
title Frontotemporal dementia.
spellingShingle Frontotemporal dementia.
Guimarães, Joana
title_short Frontotemporal dementia.
title_full Frontotemporal dementia.
title_fullStr Frontotemporal dementia.
title_full_unstemmed Frontotemporal dementia.
title_sort Frontotemporal dementia.
author Guimarães, Joana
author_facet Guimarães, Joana
Fonseca, Rosália
Garrett, Carolina
author_role author
author2 Fonseca, Rosália
Garrett, Carolina
author2_role author
author
dc.contributor.author.fl_str_mv Guimarães, Joana
Fonseca, Rosália
Garrett, Carolina
description Frontotemporal dementia (FTD), although less common than Alzheimer's, constitutes a significant percentage of the degenerative dementias, making up 8 to 17% of patients who die with dementia before the age of 70. Several clinical presentations have been described for many authors, which are included in classical behaviour disorder of frontal lobe dementia and in language alterations of progressive aphasias. Classification and diagnosis criteria's of FTP are sometime controversial in literature. So, the authors give an overview of principal's aspects in this area, with focus on clinical, imagiological, patghological and genetic perspective. Furthermore, taken in account this revision was also made a characterization of the patients followed in Dementia Outpatient Clinical Care of our hospital. In these patient characteristics review the follow parameters were analysed: FDT clinical diagnosis; demographics, clinical, imagiological, neuropsychological aspects; and disease evolution. An retrospective study that allowed correlation between some aspects, namely clinical presentation with imagiological and neuropsychological findings. With this revision work, the authors pretend to alert for the relevance of FTD diagnosis, probably misdiagnosticated.
publishDate 2007
dc.date.none.fl_str_mv 2007-01-23
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv https://www.actamedicaportuguesa.com/revista/index.php/amp/article/view/963
oai:ojs.www.actamedicaportuguesa.com:article/963
url https://www.actamedicaportuguesa.com/revista/index.php/amp/article/view/963
identifier_str_mv oai:ojs.www.actamedicaportuguesa.com:article/963
dc.language.iso.fl_str_mv por
language por
dc.relation.none.fl_str_mv https://www.actamedicaportuguesa.com/revista/index.php/amp/article/view/963
https://www.actamedicaportuguesa.com/revista/index.php/amp/article/view/963/636
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv application/pdf
dc.publisher.none.fl_str_mv Ordem dos Médicos
publisher.none.fl_str_mv Ordem dos Médicos
dc.source.none.fl_str_mv Acta Médica Portuguesa; Vol. 19 No. 4 (2006): July-August; 319-24
Acta Médica Portuguesa; Vol. 19 N.º 4 (2006): Julho-Agosto; 319-24
1646-0758
0870-399X
reponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação
instacron:RCAAP
instname_str Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação
instacron_str RCAAP
institution RCAAP
reponame_str Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
collection Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
repository.name.fl_str_mv Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação
repository.mail.fl_str_mv
_version_ 1799130622359240704