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Creutzfeldtov-Jakobov syndróm
Č. záznamu d007562 Dátum 06.06.2025 Typ M Tematický termín Creutzfeldtov-Jakobov syndróm Iný termín Angličtina (Pseudonym) New Variant Creutzfeldt-Jakob Disease
Angličtina (Pseudonym) Spongiform Encephalopathy, Subacute
Slovenčina (Pseudonym) Jakobov-Creutzfeldtov syndróm
Slovenčina (Pseudonym) vCJD
Slovenčina (Pseudonym) CJD variantná
Slovenčina (Pseudonym) Creutzfeldt-Jakobova choroba, nový variant
Slovenčina (Pseudonym) encefalopatia spongiformná subakútna
Slovenčina (Pseudonym) encefalopatia spongioformná subakútna
Slovenčina (Pseudonym) encefalopatia špongiformná subakútna
MDT C01.207.800.230C10.228.140.380.165C10.228.228.800.230F03.615.400.300 Poznámka A rare transmissible encephalopathy most prevalent between the ages of 50 and 70 years. Affected individuals may present with sleep disturbances, personality changes, ATAXIA; APHASIA, visual loss, weakness, muscle atrophy, MYOCLONUS, progressive dementia, and death within one year of disease onset. A familial form exhibiting autosomal dominant inheritance and a new variant CJD (potentially associated with ENCEPHALOPATHY, BOVINE SPONGIFORM) have been described. Pathological features include prominent cerebellar and cerebral cortical spongiform degeneration and the presence of PRIONS. (From N Engl J Med, 1998 Dec 31;339(27)) 
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