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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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| Publicado no: | Prion |
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| Main Authors: | , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Taylor & Francis
2016
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| 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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