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MALADIE CREUTZFELDT-JAKOB FAMILIALE [1 record]
Record 1 - internal organization data 2012-05-03
Record 1, English
Record 1, Subject field(s)
- Epidemiology
- Genetics
Record 1, Main entry term, English
- familial Creutzfeldt-Jakob disease
1, record 1, English, familial%20Creutzfeldt%2DJakob%20disease
correct
Record 1, Abbreviations, English
- familial CJD 2, record 1, English, familial%20CJD
correct
Record 1, Synonyms, English
Record 1, Textual support, English
Record number: 1, Textual support number: 1 DEF
Inherited form of Creutzfeldt-Jakob disease which shows an autosomal dominant pattern of disease segregation associated with a gene mutation. 1, record 1, English, - familial%20Creutzfeldt%2DJakob%20disease
Record number: 1, Textual support number: 1 OBS
If onset is usually at a slightly younger age (± 50), it generally shows clinical and pathological features analogous to the sporadic form. 1, record 1, English, - familial%20Creutzfeldt%2DJakob%20disease
Record 1, French
Record 1, Domaine(s)
- Épidémiologie
- Génétique
Record 1, Main entry term, French
- maladie de Creutzfeldt-Jakob familiale
1, record 1, French, maladie%20de%20Creutzfeldt%2DJakob%20familiale
correct, feminine noun
Record 1, Abbreviations, French
- MCJ familiale 2, record 1, French, MCJ%20familiale
correct, feminine noun
Record 1, Synonyms, French
Record 1, Textual support, French
Record number: 1, Textual support number: 1 DEF
Forme héréditaire à transmission autosomique dominante de la maladie de Creutzfeldt-Jakob associée à une mutation du gène de la prion-protéine. 1, record 1, French, - maladie%20de%20Creutzfeldt%2DJakob%20familiale
Record number: 1, Textual support number: 1 OBS
Elle survient plus précocement que la forme sporadique (âge moyen : 50 ans). D'évolution plus longue, elle présente des caractéristiques cliniques et neuropathologiques analogues à la forme sporadique. 1, record 1, French, - maladie%20de%20Creutzfeldt%2DJakob%20familiale
Record 1, Spanish
Record 1, Textual support, Spanish
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