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Neuropathic Pain in Fabry Disease

Author

Listed:
  • Hande Türker
  • Ayse Oytun Bayrak

    (Ondokuz Mayis University, Turkey)

  • Cetin Kursad Akpınar

    (Samsun Training andResearchHospital, Neurology Clinic, Turkey)

Abstract

Fabry Disease [FD] is an X-linkedly so somal storage disease caused by the mutations in the GLA gene codingforthelysosomalenzyme α-galactosidase in chromosome Xq 22.1. Thediseaseleadstoaccumulation of neutralsphingolipids in tissues. About 80% of Fabry patients [FP] suffer from a painful neuropathy that usually begins in the first two decades. About 80% of FP suffer from a painful neuropathy. Enzymereplacementtherapies with recombinant human alpagalactosidase

Suggested Citation

  • Hande Türker & Ayse Oytun Bayrak & Cetin Kursad Akpınar, 2017. "Neuropathic Pain in Fabry Disease," Open Access Journal of Neurology & Neurosurgery, Juniper Publishers Inc., vol. 2(4), pages 68-70, February.
  • Handle: RePEc:adp:joajnn:v:2:y:2017:i:4:p:68-70
    DOI: 10.19080/OAJNN.2017.02.555593
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