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
| Identifer | oai:union.ndltd.org:DRESDEN/oai:qucosa:de:qucosa:70705 |
| Date | 03 June 2020 |
| Creators | Haussmann, Robert, Wysocki, Marek, Brandt, Moritz D., Hermann, Andreas, Donix, Markus |
| Publisher | Cambridge University Press |
| Source Sets | Hochschulschriftenserver (HSSS) der SLUB Dresden |
| Language | English |
| Detected Language | English |
| Type | info:eu-repo/semantics/publishedVersion, doc-type:article, info:eu-repo/semantics/article, doc-type:Text |
| Rights | info:eu-repo/semantics/openAccess |
| Relation | 1041-6102, 1741-203X, 10.1017/S1041610216002192 |
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