Dementia due to sporadic Creutzfeldt-Jakob disease (Q65553): Difference between revisions
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Demência devida à forma mais comum de doença priônica. Tem um curso rapidamente progressivo, levando à morte em menos de 12 meses em quase todos os casos. Sintomas adicionais incluem mudanças comportamentais, descoordenação e desequilíbrio, rigidez, convulsões, espasmos mioclônicos e outros transtornos do movimento. | |||
| description / en | description / en | ||
Dementia due to the most common form of prion disease. It has a rapidly progressive course, leading to death in less than 12 months in almost all cases. Additional symptoms can include behavioural changes, incoordination and imbalance, rigidity, seizures, myoclonic jerks and other movement disorders. | |||
Revision as of 13:17, 14 August 2026
Dementia due to the most common form of prion disease. It has a rapidly progressive course, leading to death in less than 12 months in almost all cases. Additional symptoms can include behavioural changes, incoordination and imbalance, rigidity, seizures, myoclonic jerks and other movement disorders.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_2070940119 |
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| English | Dementia due to sporadic Creutzfeldt-Jakob disease |
Dementia due to the most common form of prion disease. It has a rapidly progressive course, leading to death in less than 12 months in almost all cases. Additional symptoms can include behavioural changes, incoordination and imbalance, rigidity, seizures, myoclonic jerks and other movement disorders. |
