The novel neurofilament light (NEFL) mutation Glu397Lys is associated with a clinically and morphologically heterogeneous type of Charcot-Marie-Tooth neuropathy

Stephan L Zuchner, Matthias Vorgerd, Eckhart Sindern, J. Michael Schröder

Research output: Contribution to journalArticle

71 Citations (Scopus)

Abstract

Charcot-Marie-Tooth disease comprises a heterogeneous group of hereditary neuropathies which fall into two main groups: demyelinating CMT1 with reduced nerve conduction velocity and axonal CMT2 with normal nerve conduction velocity. The neuropathological features correspond in most cases to this classification. Four genes were recently identified to cause autosomal dominant CMT2, including the neurofilament light gene. Thus far, only few mutations have been reported in neurofilament light involving eight amino acids of the gene. We identified a novel mutation, Glu397Lys, in a conserved motive signaling the end of the rod domain. The affected family members from three generations showed strikingly different clinical phenotypes, including weakness of the lower extremities, foot deformities, and deafness. The mutation was associated with nerve conduction velocities ranging from 27 m/s in a 25-year-old female to 43 m/s in an 82-year-old male in the lower extremity motor nerves. Sural nerve biopsies of two affected subjects were analyzed by light and electron microscopy. The pathological changes consisted of a reduction of predominantly large myelinated nerve fibers and various stages of onion bulb formation as typically seen in CMT1. This correlative study further confirms that neurofilament light gene mutations cause a wide clinical spectrum. Thus, analysis of the neurofilament light gene should not be restricted to pure axonal neuropathies.

Original languageEnglish
Pages (from-to)147-157
Number of pages11
JournalNeuromuscular Disorders
Volume14
Issue number2
DOIs
StatePublished - Feb 1 2004
Externally publishedYes

Fingerprint

Intermediate Filaments
Tooth
Neural Conduction
Light
Mutation
Genes
Lower Extremity
Foot Deformities
Charcot-Marie-Tooth Disease
Myelinated Nerve Fibers
Sural Nerve
Onions
Deafness
Electron Microscopy
Phenotype
Biopsy
Amino Acids

Keywords

  • Charcot-Marie-Tooth
  • Glu397Lys
  • Neurofilament light gene mutation
  • Peripheral neuropathy

ASJC Scopus subject areas

  • Clinical Neurology
  • Pediatrics, Perinatology, and Child Health
  • Developmental Neuroscience
  • Neurology

Cite this

The novel neurofilament light (NEFL) mutation Glu397Lys is associated with a clinically and morphologically heterogeneous type of Charcot-Marie-Tooth neuropathy. / Zuchner, Stephan L; Vorgerd, Matthias; Sindern, Eckhart; Schröder, J. Michael.

In: Neuromuscular Disorders, Vol. 14, No. 2, 01.02.2004, p. 147-157.

Research output: Contribution to journalArticle

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