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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| Principais autores: | , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Taylor & Francis Group
2019-01-01
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| coleção: | Prion |
| Assuntos: | |
| Acesso em linha: | https://www.tandfonline.com/doi/10.1080/19336896.2019.1651181 |
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