V180I genetic Creutzfeldt-Jakob disease with cardiac sympathetic nerve denervation masquerading as Parkinson's disease: A case report

RATIONALE: Creutzfeldt-Jakob disease (CJD) with a point mutation of valine to isoleucine at codon 180 of the prion protein gene (V180I) is the most frequent form of genetic CJD in Japan. However, peripheral nerve involvement, especially cardiac sympathetic denervation, has not been investigated in c...

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Detalles Bibliográficos
Autores principales: Fujita, Hiroaki, Ogaki, Keitaro, Shiina, Tomohiko, Onuma, Hiroki, Sakuramoto, Hirotaka, Satoh, Katsuya, Suzuki, Keisuke
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2021
Materias:
5300
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7808525/
https://www.ncbi.nlm.nih.gov/pubmed/33466217
http://dx.doi.org/10.1097/MD.0000000000024294

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7808525/
https://www.ncbi.nlm.nih.gov/pubmed/33466217
http://dx.doi.org/10.1097/MD.0000000000024294

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