Frontotemporal dementia due to GRN mutation (Q99467): Difference between revisions
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Síndrome associada à degeneração dos lobos frontal e temporal como resultado de uma mutação do gene PGRN no cromossomo 17, que codifica a Proganulina. Caracterizada por transtornos comportamentais, comprometimento cognitivo, dificuldade de linguagem e parkinsonismo. | |||
| description / en | description / en | ||
Syndrome associated with degeneration of the frontal and temporal lobes as a result of a mutation of the PGRN gene on chromosome 17 coding for Proganulin. Characterized by behavioral disturbances, cognitive impairment, language difficulty, and parkinsonism. | |||
Revision as of 16:08, 16 August 2026
Syndrome associated with degeneration of the frontal and temporal lobes as a result of a mutation of the PGRN gene on chromosome 17 coding for Proganulin. Characterized by behavioral disturbances, cognitive impairment, language difficulty, and parkinsonism.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1758869722 |
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| English | Frontotemporal dementia due to GRN mutation |
Syndrome associated with degeneration of the frontal and temporal lobes as a result of a mutation of the PGRN gene on chromosome 17 coding for Proganulin. Characterized by behavioral disturbances, cognitive impairment, language difficulty, and parkinsonism. |
