Orphanet: PRKAR1B related neurodegenerative dementia with intermediate filaments

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Disease definition

A rare, genetic neurodegenerative disease characterized by dementia and mild parkinsonism with poor levodopa response. Presenting clinical manifestations are memory problems, short attention span, disorientation, language impairment, rigidity, bradykinesia, postural instability and behavioral changes, including apathy, anxiety and delusions.

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PRKAR1B-related neurodegenerative dementia with intermediate filaments

ORPHA:412066

A summary on this disease is available in Español (2018) Français (2018) Italiano (2018) Nederlands (2018)

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