Parkinsonism due to prion diseases (Q97555): Difference between revisions
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Parkinsonismo pode ser uma característica progressiva atípica das doenças priônicas humanas, como a doença de Creutzfeldt-Jakob ou a síndrome de Gerstmann-Straussler-Scheinker. Causado por mutações pontuais na proteína príon (PRNP) que causam demência, mioclonia e ataxia. | |||
| description / en | description / en | ||
Parkinsonism can be an atypical progressive feature of human prion diseases such as Creutzfeldt–Jakob disease or Gerstmann-Straussler-Scheinker Syndrome. Caused by point mutations in prion protein (PRNP) that cause dementia, myoclonus, and ataxia. | |||
Revision as of 13:40, 16 August 2026
Parkinsonism can be an atypical progressive feature of human prion diseases such as Creutzfeldt–Jakob disease or Gerstmann-Straussler-Scheinker Syndrome. Caused by point mutations in prion protein (PRNP) that cause dementia, myoclonus, and ataxia.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_537542868 |
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| English | Parkinsonism due to prion diseases |
Parkinsonism can be an atypical progressive feature of human prion diseases such as Creutzfeldt–Jakob disease or Gerstmann-Straussler-Scheinker Syndrome. Caused by point mutations in prion protein (PRNP) that cause dementia, myoclonus, and ataxia. |
