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Scientific article
English

Ohtahara syndrome or early-onset West syndrome? A case with overlapping features and favorable response to vigabatrin

Published inEuropean journal of paediatric neurology, vol. 16, no. 6, p. 753-757
Publication date2012
Abstract

The so called "severe neonatal epilepsies with suppression-burst pattern" include early infantile epileptic encephalopathy, and early myoclonic encephalopathy. Both syndromes are characterized by pharmacoresistant seizures that appear in the first weeks (up to the third month) of life, an electroencephalographic suppression-burst pattern, and a grim prognosis. Many patients later present with other forms of epileptic encephalopathies with difficult-to-treat seizures, such as West syndrome, and those who survive usually suffer from severe neurodevelopmental troubles. We here report the case of a patient who presented at our center with features consistent with a mixed form of these epileptic encephalopathies, and favorable neurodevelopmental evolution.

Keywords
  • Anticonvulsants/therapeutic use
  • Carbamazepine/therapeutic use
  • Drug Resistance
  • Electroencephalography
  • Humans
  • Infant
  • Male
  • Neurologic Examination
  • Seizures/drug therapy/etiology
  • Spasms, Infantile/drug therapy
  • Syndrome
  • Treatment Outcome
  • Vigabatrin/therapeutic use
Citation (ISO format)
KORFF, Christian et al. Ohtahara syndrome or early-onset West syndrome? A case with overlapping features and favorable response to vigabatrin. In: European journal of paediatric neurology, 2012, vol. 16, n° 6, p. 753–757. doi: 10.1016/j.ejpn.2012.05.009
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Article (Published version)
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Identifiers
ISSN of the journal1090-3798
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