| Literature DB >> 18781290 |
H Axer1, S Hüge, C Wilhelm, M Axer, A Kunze, J R Reichenbach, M Freesmeyer, J Kohlhase, H Sauer, K-J Bär.
Abstract
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.Entities:
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Year: 2009 PMID: 18781290 DOI: 10.1007/s00115-008-2565-4
Source DB: PubMed Journal: Nervenarzt ISSN: 0028-2804 Impact factor: 1.214