Frontotemporal dementia.
Autor(a) principal: | |
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Data de Publicação: | 2007 |
Outros Autores: | , |
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. |
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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 |
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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 |
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oai:ojs.www.actamedicaportuguesa.com:article/963 |
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por |
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https://www.actamedicaportuguesa.com/revista/index.php/amp/article/view/963 https://www.actamedicaportuguesa.com/revista/index.php/amp/article/view/963/636 |
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info:eu-repo/semantics/openAccess |
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openAccess |
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application/pdf |
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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 |
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Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação |
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RCAAP |
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RCAAP |
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Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
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Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
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Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação |
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