Frontotemporal dementia due to GRN mutation (Q99467): Difference between revisions
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15 August 2026
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Latest revision as of 16:08, 16 August 2026
Syndrome associated with degeneration of the frontal and temporal lobes as a result of a mutation of the PGRN gene on chromosome 17 coding for Proganulin. Characterized by behavioral disturbances, cognitive impairment, language difficulty, and parkinsonism.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1758869722 |
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| English | Frontotemporal dementia due to GRN mutation |
Syndrome associated with degeneration of the frontal and temporal lobes as a result of a mutation of the PGRN gene on chromosome 17 coding for Proganulin. Characterized by behavioral disturbances, cognitive impairment, language difficulty, and parkinsonism. |
Statements
CID11:ID_1758869722
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dki-india-ID_1758869722
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Concluído
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15 August 2026
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