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Updated: Mar 11, 2026

Author Spotlight: Establishing a New Fluorescence-Based Protocol for In Vivo Mitochondrial Morphology Analysis in Parkinson's Disease
Published on: June 23, 2023
MAPT mutation associated with frontotemporal dementia and parkinsonism (FTDP-17)
Robert Haussmann1, Marek Wysocki1, Moritz D Brandt2
1Department of Psychiatry,University Hospital Carl Gustav Carus,Technische Universität Dresden,Dresden,Germany.
Abstract:
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.
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