Inflammatory disorders in the pathogenesis of Charcot-Marie-Tooth hereditary polyneuropathy



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Abstract

In our review, we discuss the inflammatory changes in the pathophysiology of Charcot-Marie-Tooth hereditary polyneuropathy, and this matter is still under further evaluation. Lipid oxidation, inflammatory changes, and blood inflammation agent (e.g., cytokines) concentration changes are important for the pathogenesis of this disorder. Several clinical cases of acute or chronic combination of hereditary and inflammatory polyneuropathies are identified. These clinical cases may be suspected when the typical course of Charcot-Marie-Tooth disease changed to rapid worsening of motor symptoms, inflammatory changes, and pain syndrome. Thus, anti-inflammatory treatment should be considered in these cases.

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About the authors

V B Voitenkov

Pediatric Research and Clinical Center for Infectious Diseases

E V Ekusheva

Advanced Training Institute of the Federal Medical Biological Agency

N V Skripchenko

Pediatric Research and Clinical Center for Infectious Diseases

A V Klimkin

Pediatric Research and Clinical Center for Infectious Diseases

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Copyright (c) 2018 Voitenkov V.B., Ekusheva E.V., Skripchenko N.V., Klimkin A.V.

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