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.
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complex cortical dysplasia with other brain malformations 7
MONDO:0012399
complex cortical dysplasia with other brain malformations 1
MONDO:0013541
complex cortical dysplasia with other brain malformations 2
MONDO:0014116
complex cortical dysplasia with other brain malformations 3
MONDO:0014170
complex cortical dysplasia with other brain malformations 4
MONDO:0014171
complex cortical dysplasia with other brain malformations 5
MONDO:0014337