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Idiopathic (genetic) generalized epilepsies with absences: clinical and electrographic characteristics and seizure outcome.

Ali Akbar Asadi-PooyaMaryam Homayoun
Published in: Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology (2020)
Syndromes of IGE with absences are common occurrences at epilepsy clinics. Making a syndromic diagnosis could have significant clinical implications. In doing so, interictal EEG cannot differentiate between different syndromes of IGE and the key element in making a correct syndromic diagnosis is a detailed clinical history.
Keyphrases
  • intellectual disability
  • primary care
  • working memory
  • temporal lobe epilepsy
  • genome wide