Two faces of the same coin: benign familial infantile seizures and paroxysmal kinesigenic dyskinesia caused by PRRT2 mutations

Arch Neurol. 2012 May;69(5):668-70. doi: 10.1001/archneurol.2012.187.
No abstract available

Publication types

  • Letter

MeSH terms

  • Dystonia / genetics*
  • Electroencephalography
  • Epilepsy, Benign Neonatal / genetics*
  • Family Health*
  • Female
  • Humans
  • Male
  • Membrane Proteins / genetics*
  • Mutation / genetics*
  • Nerve Tissue Proteins / genetics*

Substances

  • Membrane Proteins
  • Nerve Tissue Proteins
  • PRRT2 protein, human

Supplementary concepts

  • Convulsions benign familial neonatal dominant form
  • Familial paroxysmal dystonia