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- W2095299511 abstract "À partir d'un cas clinique, les auteurs proposent de discuter de l'état actuel des connaissances sur l'association troubles envahissants du développement et épilepsie dans la maladie de Bourneville chez l'enfant. Cette association présente un intérêt scientifique parce qu'elle laisse présager d'une participation génétique à certains troubles psychiatriques de l'enfant. Plus de 60 % des patients atteints par cette maladie génétique souffrent d'une épilepsie de topographie variable qui apparaît intriquée à des troubles d'allure autistique et à d'autres manifestations psychiatriques dont l'agressivité et l'hyperactivité. La littérature propose pour l'épilepsie, un traitement médicamenteux spécifique (carbamazépine, lamotrigine ou vigabatrin) qui n'entraverait pas le développement de l'enfant. Using a case report, the authors talk about current state of knowledge in combination of pervasive developmental disorders and epilepsy in the case of childhood tuberous sclerosis called also Bourneville's disease. This association presents a great scientific issue because it could imply a genetic link in numerous chilhood psychiatric disorders. More than 60% of patients diagnosed to have tuberous sclerosis complex suffer from seizures of different kind of topography. Epilepsy seems to be linked with autistic-like disorders and with other psychiatric disorders like aggressive and hyperactive behaviors. Concerning treatment against epilepsy, literature provides specific drug therapy (carbamazepine, lamotrigine or vigabatrin) which wouldn't damage the child mental development." @default.
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- W2095299511 date "2001-03-01" @default.
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- W2095299511 title "Maladie de Bourneville, épilepsie et troubles envahissants du développement" @default.
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- W2095299511 doi "https://doi.org/10.1016/s0222-9617(01)80018-0" @default.
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