Hypokinesia and presenile dementia in a Dutch family with a novel insertion in the prion protein gene

The clinical features and disease course of six patients from a family with autosomal dominant inheritance of presenile dementia and a hypokinetic syndrome are described. In the past, these patients have carried diagnoses of Pick's disease, Huntington's disease, Parkinson—dementia, and one patient was described as suffering from a ‘peculiar type of presenile dementia’ in a case report. In the two cases examined, the most distinctive neuropathological features were extensive globular deposits of periodic acid-Schiff plus diastase (PAS)positive material, having tinctural properties of amyloid on... Mehr ...

Verfasser: Gool, W. A. van
Hensels, G. W.
Hoogerwaard, E. M.
Wiezer, J. H. A.
Wesseling, P.
Bolhuis, P. A.
Dokumenttyp: TEXT
Erscheinungsdatum: 1995
Verlag/Hrsg.: Oxford University Press
Schlagwörter: Articles
Sprache: Englisch
Permalink: https://search.fid-benelux.de/Record/base-26632323
Datenquelle: BASE; Originalkatalog
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Link(s) : http://brain.oxfordjournals.org/cgi/content/short/118/6/1565