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Up to: Complex cortical dysplasia with other brain malformations
Polymicrogyria with optic nerve hypoplasia
A rare genetic syndrome with central nervous system malformations characterized by severe developmental delay, neonatal hypotonia, seizures, optic nerve hypoplasia and distinct central nervous system malformations including extensive bilateral polymicrogyria, dysplastic or absent corpus callosum and malformed brainstem with loss of demarcation of the pontomedullary junction.
This condition has no sub-types.