Source:http://linkedlifedata.com/resource/pubmed/id/10985702
Switch to
Predicate | Object |
---|---|
rdf:type | |
lifeskim:mentions | |
pubmed:issue |
4
|
pubmed:dateCreated |
2000-12-21
|
pubmed:abstractText |
Frontotemporal dementia (FTD) is the second most common degenerative dementia after Alzheimer's disease and its Lewy body variant. Clinical pathology can be subdivided in three main neuropathological subtypes: frontal lobe dementia, Pick's disease and FTD with motor neuron disease (MND), all characterised by distinct histological features. Until recently the presence of ubiquitin-positive intraneuronal inclusions in the dentate gyrus, and the temporal and frontal cortex was usually associated with the MND type. Such inclusions were also observed in a few sporadic cases of FTD without or with parkinsonism (FTDP) in the absence of MND. We present here clinical, neuropathological and immunohistochemical data about a Swiss FTD family with FTDP-like features but without MND. Spongiosis and mild gliosis were observed in the grey matter. No neurofibrillary tangles, Pick bodies, Lewy bodies, senile plaques or prion-positive signals were present. However, ubiquitin-positive intracytoplasmic inclusions were detected in various structures but predominantly in the dentate gyrus. These observations support the existence of a familial form of FTDP with ubiquitin-positive intracytoplasmic inclusions (Swiss FTDP family).
|
pubmed:language |
eng
|
pubmed:journal | |
pubmed:citationSubset |
IM
|
pubmed:chemical | |
pubmed:status |
MEDLINE
|
pubmed:month |
Oct
|
pubmed:issn |
0001-6322
|
pubmed:author | |
pubmed:issnType |
Print
|
pubmed:volume |
100
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
421-6
|
pubmed:dateRevised |
2007-11-9
|
pubmed:meshHeading |
pubmed-meshheading:10985702-Aged,
pubmed-meshheading:10985702-Dementia,
pubmed-meshheading:10985702-Dentate Gyrus,
pubmed-meshheading:10985702-Female,
pubmed-meshheading:10985702-Genes, Dominant,
pubmed-meshheading:10985702-Gliosis,
pubmed-meshheading:10985702-Humans,
pubmed-meshheading:10985702-Inclusion Bodies,
pubmed-meshheading:10985702-Male,
pubmed-meshheading:10985702-Motor Neurons,
pubmed-meshheading:10985702-Nerve Tissue Proteins,
pubmed-meshheading:10985702-Pedigree,
pubmed-meshheading:10985702-Switzerland,
pubmed-meshheading:10985702-Syndrome,
pubmed-meshheading:10985702-Ubiquitins
|
pubmed:year |
2000
|
pubmed:articleTitle |
Familial frontotemporal dementia with ubiquitin inclusion bodies and without motor neuron disease.
|
pubmed:affiliation |
Department of Psychiatry, University of Geneva School of Medicine, Switzerland. eniko.kovari@hcuge.ch
|
pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
|