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The clinical heterogeneity and unusual presentations of Creutzfeldt Jakob disease in Jewish patients with the PRNP codon 200 mutation

โœ Scribed by Leaver, Richard


Book ID
122398121
Publisher
Elsevier Science
Year
1992
Tongue
English
Weight
156 KB
Volume
13
Category
Article
ISSN
0197-4580

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Rhythmic pupillary oscillation in Creutz
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## Abstract We report two Creutzfeldtโ€Jakob disease (CJD) patients with rhythmic pupillary and palpebral oscillation who had a mutation of prion protein codon 200 that resulted in the substitution of lysine for glutamate (Glu/Lys). Alternating dilation and constriction of the pupils combined with e