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Research paper
Genetic and clinical characteristics of NEFL-related Charcot-Marie-Tooth disease
  1. Alejandro Horga1,2,
  2. Matilde Laurà1,3,
  3. Zane Jaunmuktane4,
  4. Nivedita U Jerath5,
  5. Michael A Gonzalez6,7,
  6. James M Polke8,9,
  7. Roy Poh8,
  8. Julian C Blake10,
  9. Yo-Tsen Liu1,11,
  10. Sarah Wiethoff12,
  11. Conceição Bettencourt12,
  12. Michael PT Lunn13,
  13. Hadi Manji1,
  14. Michael G Hanna1,
  15. Henry Houlden14,
  16. Sebastian Brandner15,
  17. Stephan Züchner16,
  18. Michael Shy5,17,
  19. Mary M Reilly1,14
  1. 1 MRC Centre for Neuromuscular Diseases, UCL Institute of Neurology, London, UK
  2. 2 Department of Neurology, Hospital Clinico Universitario San Carlos, Madrid, Spain
  3. 3 UCL Institute of Neurology, MRC Centre for Neuromuscular Diseases, National Hospital for Neurology and Neurosurgery, London, UK
  4. 4 Division of Neuropathology and Department of Neurodegenerative Disease, The National Hospital for Neurology and Neurosurgery and UCL Institute of Neurology, London, UK
  5. 5 Department of Neurology, University of Iowa, Iowa City, Iowa, USA
  6. 6 Department of Human Genetics and Hussman Institute for Human Genomics, Miller School of Medicine, University of Miami, Miami, Florida, USA
  7. 7 The Genesis Project Foundation, The Genesis Project Foundation, Miami, Florida, USA
  8. 8 Department of Neurogenetics, The National Hospital for Neurology and Neurosurgery and UCL Institute of Neurology, London, UK
  9. 9 Neurogenetics Unit, National Hospital for Neurology and Neurosurgery, London, UK
  10. 10 Department of Clinical Neurophysiology, National Hospital for Neurology and Neurosurgery (and Norfolk and Norwich University Hospital), London, UK
  11. 11 Department of Neurology, Neurological Institute, Taipei Veterans General Hospital, Taipei, Taiwan
  12. 12 Department of Molecular Neuroscience, UCL Institute of Neurology, London, UK
  13. 13 Department of Neurology, National Hospital for Neurology and Neurosurgery, London, UK
  14. 14 MRC Centre for Neuromuscular Diseases, UCL Institute of Neurology and National Hospital for Neurology and Neurosurgery, London, UK
  15. 15 Division of Neuropatholgoy, UCL Institute of Neurology and National Hospital for Neurology and Neurosurgery, London, UK
  16. 16 University of Miami, Miami, Florida, USA
  17. 17 Wayne State University, Michigan, Michigan, USA
  1. Correspondence to Professor Mary M Reilly, MRC Centre for Neuromuscular Diseases, UCL Institute of Neurology, Box 108, Queen Square, London WC1N 3BG, UK; m.reilly{at}ucl.ac.uk

Abstract

Objectives To analyse and describe the clinical and genetic spectrum of Charcot-Marie-Tooth disease (CMT) caused by mutations in the neurofilament light polypeptide gene (NEFL).

Methods Combined analysis of newly identified patients with NEFL-related CMT and all previously reported cases from the literature.

Results Five new unrelated patients with CMT carrying the NEFL mutations P8R and N98S and the novel variant L311P were identified. Combined data from these cases and 62 kindreds from the literature revealed four common mutations (P8R, P22S, N98S and E396K) and three mutational hotspots accounting for 37 (55%) and 50 (75%) kindreds, respectively. Eight patients had de novo mutations. Loss of large-myelinated fibres was a uniform feature in a total of 21 sural nerve biopsies and ‘onion bulb’ formations and/or thin myelin sheaths were observed in 14 (67%) of them. The neurophysiological phenotype was broad but most patients with E90K and N98S had upper limb motor conduction velocities <38 m/s. Age of onset was ≤3 years in 25 cases. Pyramidal tract signs were described in 13 patients and 7 patients were initially diagnosed with or tested for inherited ataxia. Patients with E90K and N98S frequently presented before age 3 years and developed hearing loss or other neurological features including ataxia and/or cerebellar atrophy on brain MRI.

Conclusions NEFL-related CMT is clinically and genetically heterogeneous. Based on this study, however, we propose mutational hotspots and relevant clinical–genetic associations that may be helpful in the evaluation of NEFL sequence variants and the differential diagnosis with other forms of CMT.

  • charcot-Marie-Tooth disease
  • NEFL
  • neurofilament light polypeptide
  • whole-exome sequencing.
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Footnotes

  • Contributors AH was involved in the study design, the acquisition, analysis and interpretation of data and drafted the manuscript. ML, ZJ, NUJ, MAG, JMP, RP, JCB, Y-TL, SW, CB, MPTL, HM, MGH, SB and HH were involved in the acquisition and interpretation of data and reviewed the manuscript. SZ and MS were involved in the study design, acquisition and interpretation of data and reviewed the manuscript. MMR supervised the study and was involved in the study design, acquisition and interpretation of data and reviewed the manuscript. All authors approved the final manuscript.

  • Competing interests None declared.

  • Ethics approval National Hospital for Neurology and Neurosurgery and UCL Institute of Neurology Ethics Committee and Institutional Review Board of the Carver College of Medicine, University of Iowa.

  • Provenance and peer review Not commissioned; externally peer reviewed.

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