Gerstmann-Straussler-Scheinker syndrome (Q38208): Difference between revisions
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13 August 2026
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Latest revision as of 02:56, 13 August 2026
A disease caused by inheritance of mutation(s) in normal prion protein genes. This disease is characterised by cerebellar ataxia, decreased coordination, dysmetria, or dysarthria, and is fatal. Confirmation is by pathological examination of the brain and genetic testing.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | 8E02.1 |
||
| English | Gerstmann-Straussler-Scheinker syndrome |
A disease caused by inheritance of mutation(s) in normal prion protein genes. This disease is characterised by cerebellar ataxia, decreased coordination, dysmetria, or dysarthria, and is fatal. Confirmation is by pathological examination of the brain and genetic testing. |
Statements
CID11:8E02.1
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dki-india-8E02.1
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Concluído
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13 August 2026
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