Familial Creutzfeldt-Jakob disease with temporal and spatial separation of affected members
Language English Country Netherlands Media print
Document type Case Reports, Journal Article
PubMed
2253724
DOI
10.1007/bf00150424
Knihovny.cz E-resources
- MeSH
- Creutzfeldt-Jakob Syndrome epidemiology etiology genetics transmission MeSH
- Middle Aged MeSH
- Humans MeSH
- Cerebral Cortex pathology MeSH
- Family MeSH
- Aged MeSH
- Animals MeSH
- Check Tag
- Middle Aged MeSH
- Humans MeSH
- Male MeSH
- Aged MeSH
- Female MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
- Case Reports MeSH
- Geographicals
- Czechoslovakia epidemiology MeSH
Familial occurrence of three definitive and two possible cases of Creutzfeldt-Jakob disease (CJD) with temporal and spatial separation in the area of focal CJD accumulation in Slovakia is reported. Incubation period is 51 and 53 years respectively, if spatial and temporal separation of affected siblings is considered, and 51 years when the time interval between the death of the affected mother and the clinical onset in the first affected child is determined. Affected children tend to die at the same time (mean difference 3.3 years) and not at the same age (mean difference 6 years). Due to separation of the affected children, a possible common exposure to CJD infection was limited to approximately seven years during their childhood. Potential endo- and exogenous risk factors and a possible mode of CJD transmission in the described family, as well as in the CJD focus, is discussed.
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