Trisomy 12p and epilepsy with myoclonic absences

Research output: Contribution to journalArticlepeer-review

Abstract

We report the case of a 6-year-2-month-old female affected by trisomy 12p syndrome. Seizures were typical myoclonic absences from both the clinical and EEG points of view. Our patient and other sporadic reports in the literature seem to support the hypothesis that, at least in some cases, myoclonic absences can be a direct or indirect effect of a chromosomopathy.

Original languageEnglish
Pages (from-to)127-130
Number of pages4
JournalBrain and Development
Volume20
Issue number2
DOIs
Publication statusPublished - Mar 1998

Keywords

  • EEG
  • Myoclonic absences
  • Trisomy 12p

ASJC Scopus subject areas

  • Clinical Neurology
  • Pediatrics, Perinatology, and Child Health
  • Neurology

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