Published online by Cambridge University Press: 20 August 2020
Malformations of cortical development (MCD) are by now well recognized causes of neurodevelopmental disorders and epilepsy [1]. The precise etiological mechanisms, clinical features and course vary as patients present with a wide range of developmental disorders, associated somatic and cortical malformations, and epilepsy. Specific clinical phenotypes can be recognized in a proportion of patients based on common clinical and imaging features. Furthermore, genetic testing allows for specific phenotype–genotype classification. However, as with many genetic disorders, the phenotypic variability is large, presenting a challenge to the diagnosis and clinical management of these patients.
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