Frontotemporal dementia due to TARDBP mutation (Q99491): Difference between revisions
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15 August 2026
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Latest revision as of 16:09, 16 August 2026
FTD due to a mutation in the gene encoding the transactive response DNA binding protein on chromosome 1. Clinically it can present as behavioural variant FTD, motor neuron disease, or FTD with motor neuron disease. Neuropathologically it is associated with TDP-43 positive inclusions.
| Language | Label | Description | Also known as |
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| default for all languages | ID_1629386211 |
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| English | Frontotemporal dementia due to TARDBP mutation |
FTD due to a mutation in the gene encoding the transactive response DNA binding protein on chromosome 1. Clinically it can present as behavioural variant FTD, motor neuron disease, or FTD with motor neuron disease. Neuropathologically it is associated with TDP-43 positive inclusions. |
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CID11:ID_1629386211
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dki-india-ID_1629386211
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Concluído
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15 August 2026
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