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Frontotemporal Dementia

Home Healthcare Now, 2022
Abstract This chapter covers frontotemporal dementia, also referred to as frontotemporal lobar degeneration, which is an umbrella term used to capture several less common forms of dementia with overlapping symptoms, microscopic changes, and genetic causes.
Katherine, Marshall, Deborah, Hale
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Frontotemporal dementia

Neurology, 1999
Abstract Nosological classification of organic dementia is based on current knowledge and theories of aetiology, including genetics, clinical picture, the pathological substrate, and the predominant location of brain damage. This chapter is concerned with dementia syndromes caused by a degenerative disease primarily affecting the frontal
Lars Gustafson, Arne Brun
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Frontotemporal dementia

Current Opinion in Neurology, 2006
The syndromes of frontotemporal lobar degeneration are increasingly recognized as an important cause of early-onset dementia. Diagnostic consensus criteria have now been established for almost a decade, and form the framework for its clinical classification.
Knibb, Jonathan A.   +2 more
  +8 more sources

FRONTOTEMPORAL DEMENTIA

Continuum, 2004
Frontotemporal dementia (FTD) is an uncommon but important form of degenerative disease. It may make up 50% of dementia cases presenting before age 60. The symptoms are related to the anatomic areas affected. Neary divided the clinical syndromes into "frontotemporal dementia," "progressive nonfluent aphasia," and "semantic dementia." However, the ...
Neill R, Graff-Radford   +1 more
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Frontotemporal Dementia

Science of Aging Knowledge Environment, 2003
In this case study, we describe the symptoms, neuropsychological testing, and brain pathology of a man with frontotemporal dementia (FTD). FTD most often presents with either a change in personality or behavior, such as social withdrawal, increased gregariousness, disinhibition, or obsessive behaviors; or with impairment of language function.
Lawrence S, Honig   +2 more
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Frontotemporal dementia

2019
Frontotemporal dementia (FTD) is the second commonest cause of young onset dementia. Our understanding of FTD and its related syndromes has advanced significantly in recent years. Among the most prominent areas of progress is the overlap between FTD, MND, and other neurodegenerative conditions at a clinicopathologic and genetic level. In parallel major
Emma M, Devenney   +2 more
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FRONTOTEMPORAL DEMENTIA

Neurologic Clinics, 2000
Frontotemporal dementia (FTD) is a unique neurodegenerative disease that can be differentiated from Alzheimer's disease and other diseases that result in cognitive complaints. The primary anatomic focus of degeneration determines the clinical presentation, which can vary from aphasia to behavioral symptoms.
H J, Rosen, J, Lengenfelder, B, Miller
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