Frontotemporal dementia due to MAPT mutation (Q99487): Difference between revisions
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DFT devida a mutação no gene codificador da MAP-tau no cromossomo 17. A apresentação clínica é geralmente de início precoce, com síndromes comportamentais ou de linguagem, com ou sem parkinsonismo. Neuropatologicamente se associa a inclusões de proteína tau, incluindo corpos de Pick. | |||||||||||||||
| description / en | description / en | ||||||||||||||
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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| Property / Canonical URI: https://id.who.int/icd/entity/105628451 / rank | |||||||||||||||
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CID11:ID_105628451 | |||||||||||||||
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dki-india-ID_105628451 | |||||||||||||||
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| Property / Knowledge Architect: https://pauloleads.com.br/cases-publicos/ / rank | |||||||||||||||
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15 August 2026
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| Property / Collection date: 15 August 2026 / rank | |||||||||||||||
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Latest 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 |
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| 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. |
Statements
CID11:ID_105628451
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dki-india-ID_105628451
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Concluído
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15 August 2026
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