Cortical sporadic Creutzfeldt-Jakob Disease (Q85595)
From determinar.ia.br - Determine suas informações
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
