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The First Sporadic Creutzfeldt–Jakob Disease Case with a Rare Molecular Subtype VV1 and 1-Octapeptide Repeat Deletion in PRNP
In the present manuscript, we report the clinical presentation and challenging diagnostic work-up of a sporadic Creutzfeldt–Jakob disease patient with confirmed VV1 subtype and heterozygous 1-octapeptide repeat deletion in the prion protein gene. The described patient was a 58-year-old woman. Intere...
Autores principales: | Areškevičiūtė, Aušrinė, Lund, Eva Løbner, Capellari, Sabina, Parchi, Piero, Pinkowsky, Christian Tersbøl |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8540765/ https://www.ncbi.nlm.nih.gov/pubmed/34696491 http://dx.doi.org/10.3390/v13102061 |
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