Cortical sporadic Creutzfeldt-Jakob Disease (Q85595): 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 | ||||||||||||||
A doença de Creutzfeldt-Jakob cortical esporádica (DCJe) é predominantemente caracterizada por demência. A proteína priônica acumulada é MM2 (MM2-cortical) e VV1, o que significa que há uma proteína priônica anormal do tipo 1 com homozigoto valina no local polimórfico do códon 129 do gene da proteína priônica. A DCJe atáxica é caracterizada por ataxia predominante e acúmulo de MV2 ou VV2. | |||||||||||||||
| description / en | description / en | ||||||||||||||
Cortical sporadic Creutzfeldt-Jakob disease (sCJD) is predominantly characterised by dementia. The accumulated prion protein is MM2 (MM2-cortical) and VV1 which means there is a type 1 abnormal prion protein with valine homozygote at codon 129 polymorphic site of prion protein gene. Ataxic sCJD is characterised by predominant ataxia and accumulation of MV2 or VV2. | |||||||||||||||
| Property / Canonical URI | |||||||||||||||
| Property / Canonical URI: https://id.who.int/icd/entity/1724965250 / rank | |||||||||||||||
Normal rank | |||||||||||||||
| Property / CURIE | |||||||||||||||
CID11:ID_1724965250 | |||||||||||||||
| Property / CURIE: CID11:ID_1724965250 / rank | |||||||||||||||
Normal rank | |||||||||||||||
| Property / Canary Token | |||||||||||||||
dki-india-ID_1724965250 | |||||||||||||||
| Property / Canary Token: dki-india-ID_1724965250 / 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 | |||||||||||||||
13 August 2026
| |||||||||||||||
| Property / Collection date: 13 August 2026 / rank | |||||||||||||||
Normal rank | |||||||||||||||
Latest revision as of 10:57, 15 August 2026
Cortical sporadic Creutzfeldt-Jakob disease (sCJD) is predominantly characterised by dementia. The accumulated prion protein is MM2 (MM2-cortical) and VV1 which means there is a type 1 abnormal prion protein with valine homozygote at codon 129 polymorphic site of prion protein gene. Ataxic sCJD is characterised by predominant ataxia and accumulation of MV2 or VV2.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1724965250 |
||
| English | Cortical sporadic Creutzfeldt-Jakob Disease |
Cortical sporadic Creutzfeldt-Jakob disease (sCJD) is predominantly characterised by dementia. The accumulated prion protein is MM2 (MM2-cortical) and VV1 which means there is a type 1 abnormal prion protein with valine homozygote at codon 129 polymorphic site of prion protein gene. Ataxic sCJD is characterised by predominant ataxia and accumulation of MV2 or VV2. |
Statements
CID11:ID_1724965250
0 references
dki-india-ID_1724965250
0 references
Concluído
0 references
13 August 2026
0 references
