EEG case report
DOI:
https://doi.org/10.25753/BirthGrowthMJ.v24.i1.8578Keywords:
epilepsy, Panayiotopoulos syndromeAbstract
Introduction: Panayiotopoulos syndrome is the second commonest idiopathic focal childhood epilepsy, with a peak of age at onset 4-5 years. Its incidence is usually underestimated, because of the typical unusual clinical manifestations of the seizures with predominant autonomic changes.
Case report: We describe a classical case of Panayiotopoulos syndrome, with recurrent seizures, but good response to antiepileptic drug treatment and remission after a few years.
Conclusion: The importance of the clinical suspicion of this epileptic syndrome and the usefulness of an electroencephalographic recording including a period of sleep is underlined. In most diagnosed cases prognosis is good, although therapy is usually necessary for a variable period of time.
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References
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Covanis A, Ferrie, CD, Koutroumanidis M, Oguni H, Panayiotopoulos CP. Panayiotopoulos syndrome and Gastaur type idiopathic childhood occipital epilepsy. In: J Roger, M Bureau, Ch. Dravet, P. Genton, C.A. Tassinari & P. Wolf. Epileptic Syndromes in Infancy, Childhood and Adolescence (4th ed.). John Libbey Eurotext Ltd 2005, pp 227-53.
Covanis A. Panayiotopoulos Syndrome: a benign childhood autonomic epilepsy frequently imitating encephalitis, syncope, migraine, sleep disorder, or gastroenteritis. Pediatrics 2006;118;e1237.
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Specchio N, Tivisano, DiCiommo, et al. Panayiotopoulos syndrome: A clinical, EEG, and neuropsychological study of 93 consecutive patients. Epilepsia 2010; 51(10):2098-107.
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