Sporadic Creutzfeldt-Jakob Disease (Q62981): Difference between revisions
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| description / pt-br | description / pt-br | ||
Doença do cérebro, que está associada a uma mutação de genes de proteínas priônicas normais ou a transformação espontânea de proteínas priônicas . Esta doença é caracterizada por um longo período de incubação, demência progressiva, déficits neurológicos e é fatal. A transmissão pode ocorrer por contato direto com tecido nervoso ou sangue infectado. A confirmação é feita por exame patológico do cérebro. | |||
| description / en | description / en | ||
A disease of the brain, that is associated with a mutation of normal prion protein genes or spontaneous transformation of prion proteins. This disease is characterised by a long incubation period, progressive dementia, neurological deficits, and is fatal. Transmission may be by direct contact with infected nervous tissue or blood. Confirmation is by pathological examination of the brain. | |||
Revision as of 10:28, 14 August 2026
A disease of the brain, that is associated with a mutation of normal prion protein genes or spontaneous transformation of prion proteins. This disease is characterised by a long incubation period, progressive dementia, neurological deficits, and is fatal. Transmission may be by direct contact with infected nervous tissue or blood. Confirmation is by pathological examination of the brain.
| Language | Label | Description | Also known as |
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| default for all languages | 8 |
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| English | Sporadic Creutzfeldt-Jakob Disease |
A disease of the brain, that is associated with a mutation of normal prion protein genes or spontaneous transformation of prion proteins. This disease is characterised by a long incubation period, progressive dementia, neurological deficits, and is fatal. Transmission may be by direct contact with infected nervous tissue or blood. Confirmation is by pathological examination of the brain. |
