Familial Creutzfeldt-Jakob disease in a patient carrying both a presenilin 1 missense substitution and a prion protein gene insertion.
J Neurol
; 247(5): 364-8, 2000 May.
Article
em En
| MEDLINE
| ID: mdl-10896268
ABSTRACT
We describe a patient who was clinically diagnosed with familial early-onset Alzheimer disease (AD) carrying both the E318G substitution in presenilin 1 (PSEN1) and an insertion of 7 octapeptide coding repeats in the prion protein gene (PRNP). Neuropathological examination revealed elongated cerebellar prion protein deposits in the absence of AD pathology. Further analysis of other family members showed that the Creutzfeldt-Jakob disease phenotype in this family was caused solely by the PRNP insertion. This observation is consistent with our previous finding that PSEN1 E318G is not causally related to AD.
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Coleções:
01-internacional
Base de dados:
MEDLINE
Assunto principal:
Príons
/
Elementos de DNA Transponíveis
/
Síndrome de Creutzfeldt-Jakob
/
Mutação de Sentido Incorreto
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Proteínas de Membrana
Limite:
Adult
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Female
/
Humans
/
Male
Idioma:
En
Ano de publicação:
2000
Tipo de documento:
Article