Chorea due to Huntington disease-like 2 (Q86512): Difference between revisions
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Doença de Huntington-like 2 é um transtorno neurodegenerativo grave que frequentemente ocorre em pacientes de origem africana, caracterizado por uma tríade de anormalidades de movimento, psiquiátricas e cognitivas. É devido a mutação no gene da junctofilina. | |||
| description / en | description / en | ||
Huntington disease-like 2 is a severe neurodegenerative disorder often occurring in patients of African origin characterized by a triad of movement, psychiatric, and cognitive abnormalities. It is due to a mutation in the junctophyllin gene. | |||
Revision as of 11:55, 15 August 2026
Huntington disease-like 2 is a severe neurodegenerative disorder often occurring in patients of African origin characterized by a triad of movement, psychiatric, and cognitive abnormalities. It is due to a mutation in the junctophyllin gene.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_187493961 |
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| English | Chorea due to Huntington disease-like 2 |
Huntington disease-like 2 is a severe neurodegenerative disorder often occurring in patients of African origin characterized by a triad of movement, psychiatric, and cognitive abnormalities. It is due to a mutation in the junctophyllin gene. |
