Frontotemporal dementia due to TARDBP mutation (Q99491): Difference between revisions
From determinar.ia.br - Determine suas informações
Changed an Item |
Changed an Item |
||||||||||||||
| (One intermediate revision by the same user not shown) | |||||||||||||||
| Property / Knowledge Architect | |||||||||||||||
| Property / Knowledge Architect: https://pauloleads.com.br/cases-publicos/ / rank | |||||||||||||||
Normal rank | |||||||||||||||
| Property / Collection date | |||||||||||||||
15 August 2026
| |||||||||||||||
| Property / Collection date: 15 August 2026 / rank | |||||||||||||||
Normal rank | |||||||||||||||
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 |
|---|---|---|---|
| default for all languages | ID_1629386211 |
||
| 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. |
Statements
CID11:ID_1629386211
0 references
dki-india-ID_1629386211
0 references
Concluído
0 references
15 August 2026
0 references
