A novel developmental encephalopathy with epilepsy and hyperkinetic movement disorders associated with a deletion of the sodium channel gene cluster on chromosome 2q24.3

Mario Mastrangelo, Davide Mei, Serena Cesario, Francesca Fioriello, Laura Bernardini, Mario Brinciotti, Renzo Guerrini, Vincenzo Leuzzi

Research output: Contribution to journalLetterpeer-review

Original languageEnglish
Pages (from-to)1-3
Number of pages3
JournalParkinsonism and Related Disorders
Publication statusPublished - Nov 1 2019


  • Developmental
  • Developmental delay
  • Dravet syndrome
  • Epileptic encephalopathies
  • Hyperkinetic movement disorders

ASJC Scopus subject areas

  • Neurology
  • Geriatrics and Gerontology
  • Clinical Neurology

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