An unusual pathologic feature and phenotype associated with familial hyperkalemic periodic paralysis

Eur J Neurol. 2008 Jun;15(6):e47-8. doi: 10.1111/j.1468-1331.2008.02135.x. Epub 2008 Apr 9.
No abstract available

Publication types

  • Case Reports
  • Letter

MeSH terms

  • Adult
  • Creatine Kinase / blood
  • Electromyography
  • Humans
  • Male
  • Muscle, Skeletal / pathology*
  • Mutation
  • Myositis / etiology
  • Myositis / pathology
  • Myositis / physiopathology
  • NAV1.4 Voltage-Gated Sodium Channel
  • Paralysis, Hyperkalemic Periodic / genetics
  • Paralysis, Hyperkalemic Periodic / pathology*
  • Paralysis, Hyperkalemic Periodic / physiopathology*
  • Pedigree
  • Phenotype*
  • Sodium Channels / genetics

Substances

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