Chronic non-paroxysmal neuropathic pain - Novel phenotype of mutation in the sodium channel SCN9A gene

Ron Dabby, Menachem Sadeh, Ronit Gilad, Yair Lampl, Sarit Cohen, Shani Inbar, Esther Leshinsky-Silver

Research output: Contribution to journalArticlepeer-review

Abstract

Background: Gain-of-function mutations in the SCN9A gene (encoding to NaV1.7 voltage-gated sodium channel) cause two rare paroxysmal pain disorders: inherited erythromelalgia (IEM) and paroxysmal extreme pain disorder (PEDP). These phenotypes are characterized by episodic extreme localized pain with cutaneous autonomic signs. So far, no other phenotypes have been associated with mutation in the SCN9A gene. Objective: To investigate mutations in the SCN9A gene in patients with chronic non-paroxysmal neuropathic pain. Patients: 9 patients with chronic severe unexplained neuropathic pain. Results: Of the nine patients one had predicted pathologic mutations in the SCN9A gene. This patient had a heterozygous change of n.4648 T-C in exon 27 resulting in a substitution of W1550R, a highly conserved amino acid, predicting damage in the transmembrane S2 region, repeat IV. This mutation was not found in 50 controls. Conclusions: SCN9A mutations cause pain syndromes other than IEM and PEPD. These mutations should be considered in patients with resistant unexplained chronic neuropathic pain.

Original languageEnglish
Pages (from-to)90-92
Number of pages3
JournalJournal of the Neurological Sciences
Volume301
Issue number1-2
DOIs
StatePublished - 15 Feb 2011

Keywords

  • Nav1.7
  • Neuropathic pain
  • SCN9A

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