Dement Neurocogn Disord.  2019 Sep;18(3):105-107. 10.12779/dnd.2019.18.3.105.

Familial Creutzfeldt–Jakob Disease with a PRNP Mutation at Codon 180 Presented with Visual Hallucinations and Illusions

Affiliations
  • 1Department of Neurology, Uijeongbu St. Mary's Hospital, The Catholic University of Korea, Uijeongbu, Korea. hyj2009@hanmail.net
  • 2Department of Neurology, Myongji Hospital, Goyang, Korea.

Abstract

No abstract available.


MeSH Terms

Codon*
Hallucinations*
Illusions*
Codon

Figure

  • Fig. 1 Diffusion weighted (upper) and fluid-attenuated inversion recovery (lower) brain magnetic resonance imaging showing high signal intensities in diffuse bilateral cortical areas.

  • Fig. 2 DNA sequences at codon 180 of prion protein gene from a normal control (left) and the patient (right). The arrow indicates a substitution of GTC (valine) by ATC (isoleucine) suggesting familial Creutzfeldt-Jakob disease.


Reference

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