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De Morsier plus syndrome: A rare congenital disorder presenting with adult onset seizure
Author(s) -
Lovelle G Ditucalan,
Herminigildo H Gan
Publication year - 2022
Language(s) - Uncategorized
Resource type - Journals
SCImago Journal Rank - 0.138
H-Index - 16
ISSN - 1823-6138
DOI - 10.54029/2022jpr
Subject(s) - polymicrogyria , septum pellucidum , schizencephaly , optic nerve hypoplasia , medicine , corpus callosum , pachygyria , agenesis of the corpus callosum , hypoplasia , cortical dysplasia , magnetic resonance imaging , pathology , pediatrics , lissencephaly , anatomy , radiology , biochemistry , chemistry , gene

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