Frontotemporal dementia due to CHMP2B mutation (Q99473): Difference between revisions
From determinar.ia.br - Determine suas informações
Created a new Item |
Changed label, description and/or aliases in pt-br, en |
||
| description / pt-br | description / pt-br | ||
Uma DFT rara de base genética, devida a uma mutação no gene codificador da "charged multivesicular body protein 2B" (CHMP2B) no cromossomo 3. Pode se apresentar como uma síndrome comportamental. Também pode estar associada a doença do neurônio motor. | |||
| description / en | description / en | ||
A rare genetic FTD due to a mutation in the gene encoding charged multivesicular body protein 2B on chromosome 3. It can present as a behavioural syndrome. It can also be associated with motor neuron disease. | |||
Revision as of 16:08, 16 August 2026
A rare genetic FTD due to a mutation in the gene encoding charged multivesicular body protein 2B on chromosome 3. It can present as a behavioural syndrome. It can also be associated with motor neuron disease.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1752271020 |
||
| English | Frontotemporal dementia due to CHMP2B mutation |
A rare genetic FTD due to a mutation in the gene encoding charged multivesicular body protein 2B on chromosome 3. It can present as a behavioural syndrome. It can also be associated with motor neuron disease. |
