MHC typing in variant Creutzfeldt-Jakob disease.
Lancet
; 361(9356): 487-9, 2003 Feb 08.
Article
em En
| MEDLINE
| ID: mdl-12583949
Identification of factors that cause susceptibility to, and clinical expression of, variant Creutzfeldt-Jakob disease (vCJD) is essential for future management of the disease. We established MHC genotypes of 76 individuals with vCJD and 131 controls, and analysed MHC phenotypes in relation to age of onset of vCJD and its duration from presentation to death. There were no significant differences between vCJD and control populations in frequencies of any MHC types, nor were there associations between MHC type and age of onset or duration of vCJD disease. Our results do not support the idea of an association between MHC types and either susceptibility to, or expression of, vCJD.
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Base de dados:
MEDLINE
Assunto principal:
Teste de Histocompatibilidade
/
Síndrome de Creutzfeldt-Jakob
/
Predisposição Genética para Doença
Tipo de estudo:
Diagnostic_studies
/
Prognostic_studies
Limite:
Adolescent
/
Adult
/
Aged
/
Child
/
Child, preschool
/
Female
/
Humans
/
Infant
/
Male
/
Middle aged
País/Região como assunto:
Europa
Idioma:
En
Revista:
Lancet
Ano de publicação:
2003
Tipo de documento:
Article