PRKAR1B-related neurodegenerative dementia with intermediate filaments

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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.

Data from Orphanet are used to provide information on a disease's name, synonym(s), and overview. Reference: Access aggregated data from Orphanet at Orphadata. Orphadata: Free access data from Orphanet. © INSERM 1999. Available on Data version June 2024

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PRKAR1B-related neurodegenerative dementia with intermediate filaments?

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Advocacy Organizations

Genetic Support Network of Victoria

The Genetic Support Network of Victoria is an organisation that supports people living with genetic, undiagnosed and rare conditions and those who support them including community and families, patient support organisations, health professionals and industry. Our vision is our community flourishing and living their best lives.

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Clinical Trials

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