Rare histotype of sporadic Creutzfeldt-Jakob disease, clinically suspected as corticobasal degeneration

Sporadic Creutzfeldt-Jakob disease (sCJD) is a rare neurodegenerative disease that can mimic other neurological disorders. We present a case of sCJD in a 64-year-old man that presented with corticobasal syndrome and survived for 3 years. He presented initially with dementia, hemiparkinsonism and ali...

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Detalles Bibliográficos
Autores principales: Tilley, Bension Shlomo, Smith, Colin, Pavese, Nicola, Attems, Johannes
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2019
Materias:
Rare Disease
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6424260/
https://www.ncbi.nlm.nih.gov/pubmed/30850568
http://dx.doi.org/10.1136/bcr-2018-228305

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6424260/
https://www.ncbi.nlm.nih.gov/pubmed/30850568
http://dx.doi.org/10.1136/bcr-2018-228305

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