[DCX-associated lissencephaly].

Abstract excerpt

We present a clinical case of a boy with lissencephaly and a pathogenic mutation in the DCX gene, detected by a molecular genetic test using next-generation sequencing (NGS). The clinical presentation, cognitive development features, and results of magnetic resonance imaging of the brain and electroencephalography are described. Also, a systematic review of the clinical, neuroimaging, and neurophysiological...

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