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Red Flags for MSA - Dansk Selskab For Geriatri

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Tauopathies<br />

Synucleinopathies<br />

Proteiner og Parkinsonisme<br />

Tauopathy with possible parkinsonism<br />

—Alzheimer’s disease<br />

Tauopathies with predominant parkinsonism<br />

—Corticobasal degeneration<br />

—Progressive supranuclear palsy<br />

—Frontotemporal dementia and parkinsonism linked to chromosome<br />

17 (FTPD-17)<br />

—Parkinsonism-dementia complex of Guam<br />

—Postencephalitic parkinsonism<br />

—Dementia pugilistica<br />

—Pantothenate kinase-associated neurodegeneration (PKAN)<br />

Other tauopathies<br />

—Pick’s disease<br />

—Down’s syndrome<br />

—Argyrophilic grain disease<br />

—Myotonic dystrophy<br />

—Dementia with tangles with or without calcification<br />

—Familial British dementia<br />

—Familial Danish dementia<br />

—Gerstmann-Straussler-Scheinker syndrome<br />

—Niemann-Pick type C disease<br />

—Subacute sclerosing panencephalitis<br />

Synucleinopathies commonly associated with dementia<br />

—Parkinson’s disease (PD)<br />

—Dementia with Lewy bodies (DLB)<br />

Other synucleinopathies<br />

—Multiple system atrophy (<strong>MSA</strong>)<br />

—Pure autonomic failure

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