Dementia due to genetic causes (Q90896): Difference between revisions
From determinar.ia.br - Determine suas informações
Changed an Item |
Changed an Item |
||||||||||||||
| Property / Collection date | |||||||||||||||
13 August 2026
| |||||||||||||||
| Property / Collection date: 13 August 2026 / rank | |||||||||||||||
Normal rank | |||||||||||||||
Latest 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 |
||
| 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). |
Statements
CID11:ID_1957030048
0 references
dki-india-ID_1957030048
0 references
Concluído
0 references
13 August 2026
0 references
