2007
DOI: 10.1186/1744-859x-6-15
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Frontotemporal Dementias: A Review

Abstract: Dementia is a clinical state characterized by loss of function in multiple cognitive domains. It is a costly disease in terms of both personal suffering and economic loss. Frontotemporal dementia (FTD) is the term now preferred over Picks disease to describe the spectrum of non-Alzheimers dementias characterized by focal atrophy of the frontal and anterior temporal regions of the brain. The prevalence of FTD is considerable, though specific figures vary among different studies. It occurs usually in an age rang… Show more

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Cited by 92 publications
(124 citation statements)
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“…Social deficits may be seen during conversational exchanges where a patient is unable to keep track of events occurring during the interaction, and thus is unable to hold a coherent conversation. Semantic dementia, also referred to as temporal variant FTD (tvFTD), is associated with predominantly temporal lobe atrophy, typically greater in the left than in the right hemisphere (Weder, Aziz, Wilkins, & Tampi, 2007). Studies involving semantic dementia patients show that the anterior temporal lobes are important for accessing knowledge of coherent concepts (Lambon Ralph, et al, 2010).…”
Section: Discussionmentioning
confidence: 99%
“…Social deficits may be seen during conversational exchanges where a patient is unable to keep track of events occurring during the interaction, and thus is unable to hold a coherent conversation. Semantic dementia, also referred to as temporal variant FTD (tvFTD), is associated with predominantly temporal lobe atrophy, typically greater in the left than in the right hemisphere (Weder, Aziz, Wilkins, & Tampi, 2007). Studies involving semantic dementia patients show that the anterior temporal lobes are important for accessing knowledge of coherent concepts (Lambon Ralph, et al, 2010).…”
Section: Discussionmentioning
confidence: 99%
“…Contudo, a frequência de mutação do gene codificador da proteína Tau nos casos de DFT esporádica é baixa. Em pacientes com histórico familiar da doença, a mutação ocorre de 9,4% a 10,5% dos casos 4,10 . Em pacientes sem o histórico familiar da demência, ocorre uma mutação de íntrons e éxons no gene da proteína Tau 25 .…”
Section: Proteína Tau Nas Doenças Degenerativasunclassified
“…Segundo as manifestações clínicas, o diagnóstico de DFT é usualmente proposto para classificar, aproximadamente, 15% a 20% das síndromes demenciais. De acordo com critérios anatomopatológicos, estima-se que 3% a 10% dos casos diagnosticados postmortem correspondem às DFTs, sendo esse número mais elevado (20%) nos casos de demência degenerativa pré-senil 4 .…”
Section: Introductionunclassified
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“…Clinical presentation often includes deficiency in performing daily activities, decrease in self-care, decrease in human relations, and change in eating habits. Disorientation, distractibility, disinhibition, perseverations, compulsive and stereotypical behaviors, and lack of insight can be observed in the psychiatric examination (4,5).Imaging studies will depict medial and anterior temporal lobe degeneration (6). Different psychiatric symptoms can be seen in FTD cases related to the affected neuroanatomical regions.…”
mentioning
confidence: 99%