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- W2017157053 abstract "A 2-month-old infant with the typical clinical features of Aicardi syndrome (i.e., infantile spasms, chorioretinal lacunae, and agenesis of the corpus callosum) is reported. At 5 years of age, pathologic examination revealed cortical heterotopias, rostral agenesis of the corpus callosum, hypoplasia of the unilateral optic nerve, and bilateral cerebellar hemispheres. Cavum septum pellucidum was present. A literature review of 5 autopsied patients with this syndrome is included." @default.
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- W2017157053 date "1989-07-01" @default.
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- W2017157053 title "Aicardi syndrome: Postmortem findings" @default.
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- W2017157053 doi "https://doi.org/10.1016/0887-8994(89)90088-x" @default.
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