Загрузка...
Diagnostic challenge of rapidly progressing sporadic Creutzfeldt-Jakob disease
Antemortem assessment of sporadic Creutzfeldt-Jakob disease (sCJD) can be significantly hampered due to its rarity, low index of clinical suspicion and its non-specific clinical features. We present an atypical case of definitive sCJD. The patient died within 5 weeks of the disease onset. This unusu...
Сохранить в:
| Опубликовано в: : | BMJ Case Rep |
|---|---|
| Главные авторы: | , |
| Формат: | Artigo |
| Язык: | Inglês |
| Опубликовано: |
BMJ Publishing Group
2019
|
| Предметы: | |
| Online-ссылка: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6768346/ https://ncbi.nlm.nih.gov/pubmed/31551319 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/bcr-2019-230535 |
| Метки: |
Добавить метку
Нет меток, Требуется 1-ая метка записи!
|