Variably protease sensitive prionopathy (Q51835): Difference between revisions
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13 August 2026
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Latest revision as of 23:03, 13 August 2026
A disease of the brain, caused by a mutation(s) in prion protein genes. This disease is characterised by deposition of abnormal prions in the brain leading to behavioural and mood changes, speech deficits, and progressive motor impairments. Confirmation is by pathological examination of the brain or identification of protease-sensitive prion proteins in a brain sample.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | 8000 |
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| English | Variably protease sensitive prionopathy |
A disease of the brain, caused by a mutation(s) in prion protein genes. This disease is characterised by deposition of abnormal prions in the brain leading to behavioural and mood changes, speech deficits, and progressive motor impairments. Confirmation is by pathological examination of the brain or identification of protease-sensitive prion proteins in a brain sample. |
Statements
CID11:8000
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dki-india-8000
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Concluído
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13 August 2026
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