Neuropathic Pain in Fabry Disease

Hande Türker, Ayse Oytun Bayrak and Cetin Kursad Akpınar
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Ayse Oytun Bayrak: Ondokuz Mayis University, Turkey
Cetin Kursad Akpınar: Samsun Training andResearchHospital, Neurology Clinic, Turkey

Open Access Journal of Neurology & Neurosurgery, 2017, vol. 2, issue 4, 68-70

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

Keywords: Open Access Journal of Neurology; Journal of Neurology & Neurosurgery; Open Access Journal; juniper publishers; neurology open access journals; journal of neurology; neurology indexed journals; neurology scholarly journals; journal of neurology; neurology journals impact factor; juniper publishers reivew (search for similar items in EconPapers)
Date: 2017
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Persistent link: https://EconPapers.repec.org/RePEc:adp:joajnn:v:2:y:2017:i:4:p:68-70

DOI: 10.19080/OAJNN.2017.02.555593

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