Prion disease resembling frontotemporal dementia and parkinsonism linked to chromosome 17
Arq. neuropsiquiatr
;
59(2A): 161-164, June 2001. ilus, tab
Artículo
en Inglés
| LILACS
| ID: lil-288609
RESUMO
OBJECTIVE:
To compare the clinical features of a familial prion disease with those of frontotemporal dementia and parkinsonism linked to chromosome 17 (FTDP-17).BACKGROUND:
Prion diseases are not usually considered in the differential diagnosis of FTDP-17, since familial Creutzfeldt-Jakob disease (CJD), the most common inherited prion disease, often manifests as a rapidly progressive dementia. Conversely, FTDP-17 usually has an insidious onset in the fifth decade, with abnormal behavior and parkinsonian features.METHOD:
We present the clinical features of 12 patients from a family with CJD associated with a point mutation at codon 183 of the prion protein gene.RESULTS:
The mean age at onset was 44.0 Ý 3.7; the duration of the symptoms until death ranged from two to nine years. Behavioral disturbances were the predominant presenting symptoms. Nine patients were first seen by psychiatrists. Eight patients manifested parkinsonian signs.CONCLUSION:
These clinical features bear a considerable resemblance to those described in FTDP-17
Texto completo:
Disponible
Índice:
LILACS (Américas)
Asunto principal:
Cromosomas Humanos Par 17
/
Síndrome de Creutzfeldt-Jakob
/
Trastornos Parkinsonianos
Tipo de estudio:
Estudio diagnóstico
Límite:
Adulto
/
Femenino
/
Humanos
/
Masculino
Idioma:
Inglés
Revista:
Arq. neuropsiquiatr
Asunto de la revista:
Neurología
/
Psiquiatria
Año:
2001
Tipo del documento:
Artículo
País de afiliación:
Brasil
/
Canadá
Institución/País de afiliación:
McGill University/CA
/
State University of Londrina/BR
/
University of Säo Paulo/BR
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