Aicardi is a rare and sporadic syndrome characterized by agenesis or dysgenesis of corpus callosum, infantile spasms and chorioretinal lacunae [5]. This syndrome is supposed to be due to a X-linked spontaneous, monogenic mutation [16]. We report a 3 month-old girl with agenesis of corpus callosum, infantile spasms, ocular abnormalities and other complex malformations.
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