A family of generalized epilepsy with febrile seizures plus type 2-a new missense mutation of SCN1A found in the pedigree of several patients with complex febrile seizures

Epilepsy Res. 2005 Feb;63(2-3):151-6. doi: 10.1016/j.eplepsyres.2004.11.005.

Abstract

We report a family with complex febrile seizures (FS). The proband is a 15-year-old boy with seizures that persisted beyond 6 years of age. His father, aunt, and cousin also have the histories of FS until 8, 9, and 8 years old, respectively. A base substitution 5569G-->T of voltage-gated sodium channel alpha-1 subunit gene was found in DNA derived from the affected members of this family.

Publication types

  • Case Reports
  • Comparative Study

MeSH terms

  • DNA Mutational Analysis / methods
  • Epilepsy, Generalized / complications
  • Epilepsy, Generalized / genetics*
  • Family Health*
  • Humans
  • Male
  • Mutation, Missense*
  • NAV1.1 Voltage-Gated Sodium Channel
  • Nerve Tissue Proteins / blood
  • Nerve Tissue Proteins / genetics*
  • Pedigree
  • Seizures, Febrile / blood
  • Seizures, Febrile / complications
  • Seizures, Febrile / genetics*
  • Sequence Homology
  • Sodium Channels / blood
  • Sodium Channels / genetics*

Substances

  • NAV1.1 Voltage-Gated Sodium Channel
  • Nerve Tissue Proteins
  • SCN1A protein, human
  • Sodium Channels