A case of V180I genetic Creutzfeldt-Jakob disease presenting with conspicuous facial mimicry
Although there have been no reports of facial mimicry in patients with Creutzfeldt-Jakob disease (CJD), we encountered a patient with genetic CJD with prion protein gene codon 180 mutation (V180I gCJD) who apparently showed this interesting clinical finding. The patient was an 87-year-old Japanese w...
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| Главные авторы: | , , , |
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| Формат: | Artigo |
| Язык: | Inglês |
| Опубликовано: |
Taylor & Francis Group
2019-01-01
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| Серии: | Prion |
| Предметы: | |
| Online-ссылка: | https://www.tandfonline.com/doi/10.1080/19336896.2019.1651181 |
| Метки: |
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