P>Lennox-Gastaut syndrome (LGS) has numerous causes, but only rarely has familial recurrence been observed. We studied a family in which three male members had severe epilepsy and intellectual disability. The proband had seizure onset at 7 years of age with atonic, myoclonic, atypical absence, and tonic seizures with slow spike-wave on electroencephalography (EEG).
Familial Lennox-Gastaut syndrome in male siblings with a novel DCX mutation and anterior pachygyria / Lawrence KM; Mei D; Newton MR; Leventer RJ; Guerrini R; Berkovic SF.. - In: EPILEPSIA. - ISSN 0013-9580. - STAMPA. - 51 (9):(2010), pp. 1902-1905. [10.1111/j.1528-1167.2010.02694.x]
Familial Lennox-Gastaut syndrome in male siblings with a novel DCX mutation and anterior pachygyria.
GUERRINI, RENZO;
2010
Abstract
P>Lennox-Gastaut syndrome (LGS) has numerous causes, but only rarely has familial recurrence been observed. We studied a family in which three male members had severe epilepsy and intellectual disability. The proband had seizure onset at 7 years of age with atonic, myoclonic, atypical absence, and tonic seizures with slow spike-wave on electroencephalography (EEG).
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