Clinical features of Creutzfeldt-Jakob disease with V180I mutation.

@article{Jin2004ClinicalFO,
  title={Clinical features of Creutzfeldt-Jakob disease with V180I mutation.},
  author={K. Gregory Jin and Yusei Shiga and Satoshi Shibuya and Kingo Chida and Yoshihiro Sato and Hidehiko Konno and Katsumi Doh-Ura and Tetsuyuki Kitamoto and Y. Itoyama},
  journal={Neurology},
  year={2004},
  volume={62 3},
  pages={502-5}
}
The authors describe the clinical features of Creutzfeldt-Jakob disease (CJD) with the causative point mutation at codon 180. The symptoms never started with visual or cerebellar involvement. The patients showed slower progression of the disease compared with sporadic CJD. They never showed periodic sharp and wave complexes in EEG. MRI demonstrated remarkable high-intensity areas with swelling in the cerebral cortex except for the medial occipital and cerebellar cortices. These characteristic… CONTINUE READING

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