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Familial Creutzfeldt-Jakob Disease: Case report and role of genetic counseling in post mortem testing

Here we present a case of an asymptomatic 53-year-old woman who sought genetic testing for Familial Creutzfeldt-Jakob Disease (fCJD) after learning that her mother had fCJD. The patient's mother had a sudden onset of memory problems and rapidly deteriorating mental faculties in her late 70s, wh...

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Detalhes bibliográficos
Publicado no:Prion
Main Authors: Clift, Kristin, Guthrie, Kimberly, Klee, Eric W., Boczek, Nicole, Cousin, Margot, Blackburn, Patrick, Atwal, Paldeep
Formato: Artigo
Idioma:Inglês
Publicado em: Taylor & Francis 2016
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC5161295/
https://ncbi.nlm.nih.gov/pubmed/27929804
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1080/19336896.2016.1254858
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