Sporadic Creutzfeldt-Jakob Disease in a Young Girl With Unusually Long Survival

Author:

D’Arcy Colleen E1,Bitnun Ari2,Coulthart Michael B3,D’Amour Rolande3,Friedman Jeremy4,Knox J David5,Rapoport Adam2,Carter Snead6,Widjaja Elysa7,Hazrati Lili-Naz1,Jansen Gerard H8

Affiliation:

1. Division of Pathology, The Hospital for Sick Children, Toronto, Ontario, Canada

2. Department of Pediatrics, University of Toronto, Toronto, Ontario, Canada

3. Canadian Creutzfeldt-Jakob Disease Surveillance System, Public Health Agency of Canada, Ottawa, Canada

4. Division of Pediatric Medicine, Department of Pediatrics, The Hospital for Sick Children, University of Toronto, Toronto, Ontario, Canada

5. National Microbiology Laboratory, Public Health Agency of Canada, Winnipeg, Manitoba, Canada

6. Department of Family and Community Medicine, University of Toronto, Toronto, Ontario, Canada

7. Diagnostic Imaging, The Hospital for Sick Children, Toronto, Ontario, Canada

8. Department of Pathology and Laboratory Medicine, University of Ottawa, Ottawa, Canada

Publisher

Oxford University Press (OUP)

Subject

Cellular and Molecular Neuroscience,Clinical Neurology,Neurology,General Medicine,Pathology and Forensic Medicine

Reference16 articles.

1. Prions;Prusiner;Proc Natl Acad Sci USA,1998

2. The end of the BSE saga: Do we still need surveillance for human prion diseases?;Budka;Swiss Med Wkly,2015

3. Predictors of survival in sporadic Creutzfeldt-Jakob disease and other human transmissible spongiform encephalopathies;Pocchiari;Brain,2004

4. Panencephalopathic type of Creutzfeldt-Jakob disease: Primary involvement of the cerebral white matter;Mizutani;J Neurol Neurosurg Psychiatry,1981

5. Panencephalopathic Creutzfeldt-Jakob disease in the Netherlands and the UK: Clinical and pathological characteristics of nine patients;Jansen;Neuropathol Appl Neurobiol,2009

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