Brain 18F-FDG PET/CT findings in a case of genetic Creutzfeldt-Jakob disease due to V203I heterozygous mutation in the PRNP gene.

Authors :: Cistaro A
Cassalia L
Ferrara C
Atzori C
Vai D
Quartuccio N
Fania P
Vaudano GP
Imperiale D
Source :: Journal of neurology [J Neurol] 2017 Jan; Vol. 264 (1), pp. 170-173. Date of Electronic Publication: 2016 Nov 14.
Publication Year :: 2017

Subjects :: Brain metabolism
Creutzfeldt-Jakob Syndrome metabolism
Female
Fluorodeoxyglucose F18
Heterozygote
Humans
Middle Aged
Radiopharmaceuticals
Brain diagnostic imaging
Creutzfeldt-Jakob Syndrome diagnostic imaging
Creutzfeldt-Jakob Syndrome genetics
Mutation
Positron Emission Tomography Computed Tomography
Prion Proteins genetics

Full Text Access

Tools