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Creutzfeldt–Jakob disease with E200KPRNPmutation: a case report and revision of the literature

✍ Scribed by Michelangelo Mancuso; Gabriele Siciliano; Sabina Capellari; Daniele Orsucci; Policarpo Moretti; Giuseppe Di Fede; Silvia Suardi; Rosaria Strammiello; Piero Parchi; Fabrizio Tagliavini; Luigi Murri

Publisher
Springer Milan
Year
2009
Tongue
English
Weight
256 KB
Volume
30
Category
Article
ISSN
1590-1874

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Creutzfeldt-Jakob disease: a case with e
Creutzfeldt-Jakob disease: a case with extensive white matter degeneration and optic atrophy
✍ Y. Kitagawa; F. Gotoh; A. Koto; S. Ebihara; H. Okayasu; T. Ishii; H. Matsuyama 📂 Article 📅 1983 🏛 Springer 🌐 English ⚖ 881 KB

A 52-year-old woman is described, whose clinical features were typical of Creutzfeldt-Jakob disease except for the presence of optic atrophy. Serial CT scans showed rapid development of brain atrophy early in the course. Postmortem examination revealed extensive degeneration of the cerebral and cere