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