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...

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Detalles Bibliográficos
Autores principales: Areškevičiūtė, Aušrinė, Lund, Eva Løbner, Capellari, Sabina, Parchi, Piero, Pinkowsky, Christian Tersbøl
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Case Report
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

Internet

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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