Clinical features of familial Creutzfeldt-Jakob disease and the E200K mutation in Spain

Creutzfeldt-Jakob disease (CJD) is an infrequent pathology affecting the central nervous system (about 1/1,000000) that has a subacute progression and, for the time being, a fatal prognosis. The familial forms account for between 5-10% of cases and one of the most frequent is that produced by the E2...

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Veröffentlicht in:	Revista de neurologiá 2007-02, Vol.44 (3), p.150-153
Hauptverfasser:	Morgado-Linares, R Y, Ruiz-Peña, J L, Páramo, M D, Díaz-Delgado, M, Izquierdo, G
Format:	Artikel
Sprache:	spa
Schlagworte:	Creutzfeldt-Jakob Syndrome - diagnosis Creutzfeldt-Jakob Syndrome - genetics Creutzfeldt-Jakob Syndrome - pathology Creutzfeldt-Jakob Syndrome - physiopathology Fatal Outcome Female Humans Middle Aged Mutation Pedigree Prions - genetics Spain
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