Severe Myoclonic Epilepsy of Infancy (SMEI) or Dravet syndrome is a rare epileptic encephalopathy with onset within the first year of life manifesting in 1:30.000 subjects. Epileptic manifestations are associated to progressive neurocognitive deterioration and verbal speech impairment. The epileptic history and semiology, the electroencephalographic pattern, the genotype and pharmacological treatment of a group of six Italian pazients with SMEI were retrospectuvely analyzed.
EPILESSIA MIOCLONICA SEVERA DELL’INFANZIA: STUDIO DI FOLLOW-UP DI UN CAMPIONE DI SOGGETTI DALLA PRIMA INFANZIA ALL’ETÀ ADULTA.
DI ROSA, GABRIELLA;TORTORELLA, Gaetano
2011-01-01
Abstract
Severe Myoclonic Epilepsy of Infancy (SMEI) or Dravet syndrome is a rare epileptic encephalopathy with onset within the first year of life manifesting in 1:30.000 subjects. Epileptic manifestations are associated to progressive neurocognitive deterioration and verbal speech impairment. The epileptic history and semiology, the electroencephalographic pattern, the genotype and pharmacological treatment of a group of six Italian pazients with SMEI were retrospectuvely analyzed.File in questo prodotto:
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