Demyelinating peripheral neuropathy in Creutzfeldt–Jakob disease

Miriam Y. Neufeld; Joseph Josiphov; Amos D. Korczyn

doi:10.1002/mus.880151103

Demyelinating peripheral neuropathy in Creutzfeldt–Jakob disease

Miriam Y. Neufeld, Joseph Josiphov, Amos D. Korczyn^*

^*Corresponding author for this work

Tel Aviv University

Research output: Contribution to journal › Article › peer-review

60 Scopus citations

Abstract

We desribe 2 patients of Jewish Libyan descent, who presented with a clinical syndrome compatible with Creutzfeldt–Jakob disease and who were found to have a mutation of codon 200 in the prion protein. The patients developed symptoms and signs of peripheral nerve involvement diagnosed by electrodiagnostic and histopathological studies as demyelinating neuropathy. This may be a rare manifestation of Creutzfeldt–Jakob disease. © 1992 John Wiley & Sons, Inc.

Original language	English
Pages (from-to)	1234-1239
Number of pages	6
Journal	Muscle and Nerve
Volume	15
Issue number	11
DOIs	https://doi.org/10.1002/mus.880151103
State	Published - Nov 1992

Keywords

Creutzfeldt–Jakob disease
demyelinating neuropathy
peripheral neuropathy
peripheral neuropathy
prions

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This output contributes to the following UN Sustainable Development Goals (SDGs)

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10.1002/mus.880151103

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Demyelinating peripheral neuropathy in Creutzfeldt–Jakob disease

Abstract

Keywords

UN SDGs

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