Dementia due to genetic causes (Q90896): Difference between revisions
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Demência devida a infartos cerebrais associados a mutações genéticas. Podem ser autossômicas dominantes (como a CADASIL, decorrente da mutação Notch3) ou autossômicas recessivas (como a CARASIL, decorrente da mutação HTRA1). | |||
| description / en | description / en | ||
Dementia that is due to cerebral infarcts associated with a genetic mutations. They can be autosomal dominant (such as CADASIL due to Notch3 mutation) or autosomal recessive (such as CARASIL due to HTRA1 mutation). | |||
Revision as of 17:53, 15 August 2026
Dementia that is due to cerebral infarcts associated with a genetic mutations. They can be autosomal dominant (such as CADASIL due to Notch3 mutation) or autosomal recessive (such as CARASIL due to HTRA1 mutation).
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1957030048 |
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| English | Dementia due to genetic causes |
Dementia that is due to cerebral infarcts associated with a genetic mutations. They can be autosomal dominant (such as CADASIL due to Notch3 mutation) or autosomal recessive (such as CARASIL due to HTRA1 mutation). |
