" /> Sporadic Creutzfeldt-Jakob Disease - CISMeF





ICD-11 code : 8E00;

Preferred Label : Sporadic Creutzfeldt-Jakob Disease;

ICD-11 definition : 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 characterized 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.;

ICD-11 synonym : Creutzfeld-Jakob disease NOS; idiopathic Creutzfeldt-Jakob disease; sCJD - [Sporadic Creutzfeldt-Jakob Disease]; sCJD;

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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 characterized 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.

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29/07/2025


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