Partial epilepsy and 47,XXX karyotype: report of four cases

Pediatr Neurol. 2006 Jul;35(1):69-74. doi: 10.1016/j.pediatrneurol.2006.01.003.

Abstract

Epilepsy is a common finding in chromosomal imbalances, but only a few chromosome abnormalities have a characteristic electro-clinical pattern. Trisomy X is one of the most common sex chromosome abnormalities in females, and is associated with considerable phenotypic variability. This report describes four 47,XXX females with mental deficiency and epilepsy. Although a specific electro-clinical pattern could not be defined, the epileptic phenotypes of these patients share many features; we suggest that the association 47,XXX/epilepsy/mental retardation may not be coincidental. This report also enlarges the clinical spectrum of the 47,XXX phenotype. Moreover, these observations highlight the critical role of chromosome X in epilepsy and mental retardation.

Publication types

  • Case Reports

MeSH terms

  • Child, Preschool
  • Chromosome Aberrations
  • Chromosomes, Human, X / genetics*
  • Epilepsies, Partial / diagnosis
  • Epilepsies, Partial / genetics*
  • Epilepsies, Partial / physiopathology
  • Female
  • Humans
  • Infant
  • Trisomy / diagnosis*
  • Trisomy / genetics*