Fatal insomnia in a case of familial Creutzfeldt-Jakob disease with the codon 200Lys mutation

J. Chapman*, A. Arlazoroff, L. G. Goldfarb, L. Cervenakova, M. Y. Neufeld, E. Werber, M. Herbert, P. Brown, D. C. Gajdusek, A. D. Korczyn

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

Abstract

Fatal familial insomnia (FFI) has been exclusively associated with a pathogenic mutation at codon 178 in the PRNP gene coupled with methionine (Met) at codon 129. We now describe a subject with familial Creutzfeldt-Jakob disease, heterozygous for the pathogenic lysine (Lys) mutation at codon 200 and homozygous for Met at codon 129 of the PRNP gene, who was affected by severe insomnia. At autopsy the patient had significant involvement of the thalamus, as previously described in subjects affected by FFI with the codon 178 mutation. This case demonstrates the wide variability of the clinical expressions in patients with the codon 200 mutation, that may include insomnia and thalamic pathology.

Original languageEnglish
Pages (from-to)758-761
Number of pages4
JournalNeurology
Volume46
Issue number3
DOIs
StatePublished - Mar 1996

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