Frontotemporal dementia due to MAPT mutation (Q99487): Difference between revisions
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Revision as of 16:09, 16 August 2026
FTD due to a mutation in the gene encoding MAP-tau on chromosome 17. Clinical presentation is usually early onset, with behavioural or language syndromes, with or without Parkinsonism. Neuropathologically it is associated with tau inclusions including Pick bodies.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_105628451 |
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| English | Frontotemporal dementia due to MAPT mutation |
FTD due to a mutation in the gene encoding MAP-tau on chromosome 17. Clinical presentation is usually early onset, with behavioural or language syndromes, with or without Parkinsonism. Neuropathologically it is associated with tau inclusions including Pick bodies. |
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CID11:ID_105628451
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dki-india-ID_105628451
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Concluído
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