frontotemporal lobar degenerations การใช้

• Frontotemporal lobar degeneration and Huntington's disease account for most of the remaining cases.
• Among people with frontotemporal lobar degeneration, more than half ( 60 % ) had stereotypies.
• SD is one of the three canonical clinical syndromes associated with frontotemporal lobar degeneration ( FTLD ).
• The clinical diagnosis of KL was temporal variant frontotemporal lobar degeneration with progressive right temporal lobe atrophy.
• Hyperreligiosity may occur in a variety of disorders including epilepsy, psychotic disorders and frontotemporal lobar degeneration.
• The time to onset of stereotypies in people with frontotemporal lobar degeneration may be years ( average 2.1 years ).
• PiD has several unique biochemical characteristics that allow for identification of Pick s disease as opposed to other pathological subtypes of frontotemporal lobar degeneration.
• Frontotemporal lobar degeneration ( FTLD ) is a neurodegenerative disease that attacks the brain selectively in the frontal lobe, temporal lobe and amygdala.
• Hyperreligiosity may be associated with epilepsy, in particular temporal lobe epilepsy, complex partial seizures, mania, frontotemporal lobar degeneration, and psychotic disorder.
• She has also studied diseases including Lewy Body disease, Parkinson's disease, progressive supranuclear palsy, multiple system atrophy, frontotemporal lobar degeneration, and corticobasal degeneration.
• However, relatives of a person with any form of frontotemporal lobar degeneration, including PPA, are at slightly greater risk of developing PPA or another form of the condition.
• Mutations in the " GRN " gene have been implicated in up to 25 % of frontotemporal lobar degeneration, inherited in an autosomal dominant fashion with high penetrance.
• What If It s Not Alzheimer s ? is the first and only comprehensive guide dealing with frontotemporal lobar degeneration ( FTLD ), one of the largest groups of non-Alzheimer s dementias.
• The non-Alzheimer's tauopathies are sometimes grouped together as " "'Pick's complex "'" because of their association with Frontotemporal dementia, or Frontotemporal lobar degeneration.
• With regards to the genetic defects that have been found, repeat expansion in the C9orf72 gene is considered a major contribution to frontotemporal lobar degeneration, although defects in the MAPT genes are also associated with it.
• For > 15 years, Dr . Trojanowski has conducted research on AD, PD, motor neuron disease, dementia with Lewy bodies ( DLB ), frontotemporal lobar degeneration ( FTLD ) and other aging related nervous system disorders.
• Some people use the term Pick's disease to mean the more general clinical syndrome of frontotemporal lobar degeneration, but this has previously led to confusion among professionals and patients and so its use should be restricted to the specific pathological subtype described below.
• While the term " Pick's disease " was once used to represent a class of clinical syndromes with symptoms attributable to frontal and temporal lobe dysfunction, it is now used among professionals to mean a specific pathology that is one of the causes of frontotemporal lobar degeneration.
• The disease entities which are now considered subtypes of FTLD-FUS are atypical frontotemporal lobar degeneration with ubiquitinated inclusions ( aFTLD-U ), NIFID ( otherwise known as neurofilament inclusion body disease ) and basophilic inclusion body disease ( BIBD ), which together with ALS-FUS comprise the FUS-opathies.
• "' Frontotemporal dementia "'( "'FTD "') is the clinical presentation of frontotemporal lobar degeneration, which is characterized by progressive neuronal loss predominantly involving the frontal and / or temporal lobes, and typical loss of over 70 % of spindle neurons, while other neuron types remain intact.