Dementia due to Fragile X Syndrome (Q99872): Difference between revisions
From determinar.ia.br - Determine suas informações
Created a new Item |
Changed an Item |
||||||||||||||
| (6 intermediate revisions by the same user not shown) | |||||||||||||||
| description / pt-br | description / pt-br | ||||||||||||||
Demência devida à síndrome do X frágil, uma síndrome genética rara caracterizada por tremor intencional, ataxia, parkinsonismo, alterações cognitivas e comportamentais. É uma doença de corpos de inclusão com inclusões intranucleares em todo o cérebro, particularmente no hipocampo e no córtex frontal, bem como nos núcleos cerebelares profundos. Alguns caracterizaram a demência como sendo do subtipo subcortical frontal. | |||||||||||||||
| description / en | description / en | ||||||||||||||
Dementia due to Fragile X Syndrome, a rare genetic syndrome characterised by intention tremor, ataxia, parkinsonism, cognitive and behavioural changes. It is an inclusion body disease with intranuclear inclusions throughout the brain, particularly in the hippocampus and frontal cortex, as well as in the deep cerebellar nuclei. Some have characterised the dementia as one of frontal subcortical subtype. | |||||||||||||||
| Property / Canonical URI | |||||||||||||||
| Property / Canonical URI: https://id.who.int/icd/entity/874230470 / rank | |||||||||||||||
Normal rank | |||||||||||||||
| Property / CURIE | |||||||||||||||
CID11:ID_874230470 | |||||||||||||||
| Property / CURIE: CID11:ID_874230470 / rank | |||||||||||||||
Normal rank | |||||||||||||||
| Property / Canary Token | |||||||||||||||
dki-india-ID_874230470 | |||||||||||||||
| Property / Canary Token: dki-india-ID_874230470 / rank | |||||||||||||||
Normal rank | |||||||||||||||
| Property / Verification Status | |||||||||||||||
Concluído | |||||||||||||||
| Property / Verification Status: Concluído / rank | |||||||||||||||
Normal rank | |||||||||||||||
| Property / Knowledge Architect | |||||||||||||||
| Property / Knowledge Architect: https://pauloleads.com.br/cases-publicos/ / rank | |||||||||||||||
Normal rank | |||||||||||||||
| Property / Collection date | |||||||||||||||
15 August 2026
| |||||||||||||||
| Property / Collection date: 15 August 2026 / rank | |||||||||||||||
Normal rank | |||||||||||||||
Latest revision as of 16:33, 16 August 2026
Dementia due to Fragile X Syndrome, a rare genetic syndrome characterised by intention tremor, ataxia, parkinsonism, cognitive and behavioural changes. It is an inclusion body disease with intranuclear inclusions throughout the brain, particularly in the hippocampus and frontal cortex, as well as in the deep cerebellar nuclei. Some have characterised the dementia as one of frontal subcortical subtype.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_874230470 |
||
| English | Dementia due to Fragile X Syndrome |
Dementia due to Fragile X Syndrome, a rare genetic syndrome characterised by intention tremor, ataxia, parkinsonism, cognitive and behavioural changes. It is an inclusion body disease with intranuclear inclusions throughout the brain, particularly in the hippocampus and frontal cortex, as well as in the deep cerebellar nuclei. Some have characterised the dementia as one of frontal subcortical subtype. |
Statements
CID11:ID_874230470
0 references
dki-india-ID_874230470
0 references
Concluído
0 references
15 August 2026
0 references
