Alternating hemiplegia and paroxysmal torticollis caused by SCN4A mutation: A new phenotype?

Neurology. 2019 Oct 8;93(15):673-674. doi: 10.1212/WNL.0000000000008212. Epub 2019 Sep 6.
No abstract available

Publication types

  • Case Reports

MeSH terms

  • Child, Preschool
  • Hemiplegia / complications
  • Hemiplegia / genetics*
  • Humans
  • Male
  • Mutation / genetics*
  • NAV1.4 Voltage-Gated Sodium Channel / genetics*
  • Phenotype
  • Torticollis / complications
  • Torticollis / genetics*

Substances

  • NAV1.4 Voltage-Gated Sodium Channel
  • SCN4A protein, human

Supplementary concepts

  • Alternating hemiplegia of childhood