Frontotemporal dementia due to TARDBP mutation (Q99491): Difference between revisions
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DFT devida a uma mutação no gene codificador da "transactive response DNA binding protein" no cromossomo1. Pode se apresentar clinicalmente como a variante comportamental da DFT, doença do neurônio motor, ou DFT com doença do neurônio motor. Neuropatologicamente, está associada com inclusões positivas para TDP-43. | |||
| description / en | description / en | ||
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. | |||
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. |
