Source:http://linkedlifedata.com/resource/pubmed/id/18781290
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
1
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pubmed:dateCreated |
2009-2-12
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pubmed:abstractText |
We report a patient with early-onset autosomal dominant dementia. The CSF showed increased levels of tau protein and decreased amyloid beta (ratio 42:40) typical for Alzheimer's disease. Cerebral MRI revealed vascular lesions and white-matter changes around the posterior horns of the ventricles with only moderate atrophy of the brain. Susceptibility-weighted imaging detected multiple small hemorrhagic changes. Gene analysis revealed amyloid precursor protein (APP) locus duplication as the cause of hereditary Alzheimer's dementia. The co-occurrence of CSF changes typical for Alzheimer's disease and MRI findings of cerebral amyloid angiopathy is remarkable, as it is also described for APP locus duplication. In conjunction with a family history suggestive of hereditary dementia, such a constellation should lead to enhanced gene analysis.
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pubmed:language |
ger
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Jan
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pubmed:issn |
1433-0407
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pubmed:author | |
pubmed:issnType |
Electronic
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pubmed:volume |
80
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
62-3, 65-7
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pubmed:dateRevised |
2010-11-18
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pubmed:meshHeading |
pubmed-meshheading:18781290-Alzheimer Disease,
pubmed-meshheading:18781290-Amyloid beta-Peptides,
pubmed-meshheading:18781290-Heterozygote,
pubmed-meshheading:18781290-Humans,
pubmed-meshheading:18781290-Male,
pubmed-meshheading:18781290-Middle Aged,
pubmed-meshheading:18781290-Pedigree,
pubmed-meshheading:18781290-Peptide Fragments
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pubmed:year |
2009
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pubmed:articleTitle |
[Hereditary Alzheimer's disease with amyloid angiopathy caused by amyloid precursor protein locus].
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pubmed:affiliation |
Klinik für Psychiatrie und Psychotherapie, Friedrich-Schiller-Universität, Jena, Deutschland. Hubertus.Axer@med.uni-jena.de
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pubmed:publicationType |
Journal Article,
English Abstract,
Case Reports
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