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. | |||
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. |
