Cargando...
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...
Gardado en:
| Publicado en: | Prion |
|---|---|
| Main Authors: | , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado: |
Taylor & Francis
2019
|
| Assuntos: | |
| Acceso en liña: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6746545/ https://ncbi.nlm.nih.gov/pubmed/31387445 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1080/19336896.2019.1651181 |
| Tags: |
Engadir etiqueta
Sen Etiquetas, Sexa o primeiro en etiquetar este rexistro!
|