Cortical sporadic Creutzfeldt-Jakob Disease (Q85595): Difference between revisions
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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 |
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| 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. |
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CID11:ID_1724965250
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