Table of Contents Author Guidelines Submit a Manuscript
Case Reports in Neurological Medicine
Volume 2013 (2013), Article ID 243652, 4 pages
http://dx.doi.org/10.1155/2013/243652
Case Report

Central Nervous System Demyelination in a Charcot-Marie-Tooth Type 1A Patient

1st Department of Neurology, Athens National University, “Aeginition” Hospital, 74 Vas. Sophia’s Avenue, 11528 Athens, Greece

Received 22 October 2013; Accepted 11 November 2013

Academic Editors: R. Hashimoto, M. Swash, and Y. Wakabayashi

Copyright © 2013 Christos Koros et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Linked References

  1. T. Zambelis, M. Panas, P. Kokotis, G. Karadima, E. Kararizou, and N. Karandreas, “Central motor and sensory pathway involvement in an X-linked Charcot-Marie-Tooth family,” Acta Neurologica Belgica, vol. 108, no. 2, pp. 44–47, 2008. View at Google Scholar · View at Scopus
  2. G. Isoardo, N. Di Vito, M. Nobile, G. Benetton, and F. Fassio, “X-linked Charcot-Marie-Tooth disease and progressive-relapsing central demyelinating disease,” Neurology, vol. 65, no. 10, pp. 1672–1673, 2005. View at Publisher · View at Google Scholar · View at Scopus
  3. P. K. Thomas, “Overview of Charcot-Marie-Tooth disease type 1A,” Annals of the New York Academy of Sciences, vol. 883, pp. 1–5, 1999. View at Google Scholar · View at Scopus
  4. K. Rezania, B. G. Arnason, and B. Soliven, “Patterns and significance of concomitant central and peripheral inflammatory demyelination,” Neurological Research, vol. 28, no. 3, pp. 326–333, 2006. View at Publisher · View at Google Scholar · View at Scopus
  5. N. Kawamura, R. Yamasaki, T. Yonekawa et al., “Anti-neurofascin antibody in patients with combined central and peripheral demyelination,” Neurology, vol. 81, pp. 714–722, 2013. View at Google Scholar
  6. D. H. Kilfoyle, P. J. Dyck, Y. Wu et al., “Myelin protein zero mutation His39Pro: hereditary motor and sensory neuropathy with variable onset, hearing loss, restless legs and multiple sclerosis,” Journal of Neurology, Neurosurgery and Psychiatry, vol. 77, no. 8, pp. 963–966, 2006. View at Publisher · View at Google Scholar · View at Scopus
  7. E. Frasson, A. Polo, A. Di Summa et al., “Multiple sclerosis associated with duplicated CMT1A: a report of two cases,” Journal of Neurology Neurosurgery and Psychiatry, vol. 63, no. 3, pp. 413–414, 1997. View at Google Scholar · View at Scopus
  8. M. Panas, G. Karadima, N. Kalfakis, P. Floroskufi, and D. Vassilopoulos, “Charcot-Marie-Tooth disease type 1A with central nervous system involvement in two generations,” Journal of Neurology, vol. 251, no. 4, pp. 484–485, 2004. View at Publisher · View at Google Scholar · View at Scopus
  9. M. Almsaddi, T. E. Bertorini, and W. K. Seltzer, “Demyelinating neuropathy in a patient with multiple sclerosis and genotypical HMSN-1,” Neuromuscular Disorders, vol. 8, no. 2, pp. 87–89, 1998. View at Publisher · View at Google Scholar · View at Scopus
  10. B. R. Wakerley, F. E. Harman, D. M. Altmann, and O. Malik, “Charcot-Marie-Tooth disease associated with recurrent optic neuritis,” Journal of Clinical Neuroscience, vol. 18, no. 10, pp. 1422–1423, 2011. View at Publisher · View at Google Scholar · View at Scopus
  11. Y. Ohsawa, T. Murakami, Y. Miyazaki, T. Shirabe, and Y. Sunada, “Peripheral myelin protein 22 is expressed in human central nervous system,” Journal of the Neurological Sciences, vol. 247, no. 1, pp. 11–15, 2006. View at Publisher · View at Google Scholar · View at Scopus