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MAPT mutation associated with frontotemporal dementia and parkinsonism (FTDP-17)

We present a 56-year-old patient suffering from frontotemporal dementia with parkinsonism linked to chromosome 17 (FTDP-17). The history included a three-generation pedigree and the patient was found to be a mutation carrier. The diagnosis was hindered by late appearance of the hypokinetic movement disorder. For clinicians, it is important to consider rare neurodegenerative disease variants in early-onset familial dementia syndromes with behavioral, cognitive, and motor symptoms

Identiferoai:union.ndltd.org:DRESDEN/oai:qucosa:de:qucosa:70705
Date03 June 2020
CreatorsHaussmann, Robert, Wysocki, Marek, Brandt, Moritz D., Hermann, Andreas, Donix, Markus
PublisherCambridge University Press
Source SetsHochschulschriftenserver (HSSS) der SLUB Dresden
LanguageEnglish
Detected LanguageEnglish
Typeinfo:eu-repo/semantics/publishedVersion, doc-type:article, info:eu-repo/semantics/article, doc-type:Text
Rightsinfo:eu-repo/semantics/openAccess
Relation1041-6102, 1741-203X, 10.1017/S1041610216002192

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