Frontotemporal dementia due to VCP mutation (Q99478): Difference between revisions
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DFT devida a mutações na proteína contendo valosina no cromossomo 9. Também está associada a miosite por corpos de inclusão e doença óssea de Paget, bem como doença do neurônio motor. Neuropatologicamente ocorrem inclusões positivas para ubiquitina. | |||
| description / en | description / en | ||
FTD due to mutations in the valosin-containing protein on chromosome 9. It is also associated with inclusion body myositis and Paget's disease of the bone, as well as motor neuron disease. Neuropathologically there are ubiquitin positive inclusions | |||
Revision as of 16:08, 16 August 2026
FTD due to mutations in the valosin-containing protein on chromosome 9. It is also associated with inclusion body myositis and Paget's disease of the bone, as well as motor neuron disease. Neuropathologically there are ubiquitin positive inclusions
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1650171830 |
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| English | Frontotemporal dementia due to VCP mutation |
FTD due to mutations in the valosin-containing protein on chromosome 9. It is also associated with inclusion body myositis and Paget's disease of the bone, as well as motor neuron disease. Neuropathologically there are ubiquitin positive inclusions |
