Korean J Pediatr.  2017 Jan;60(1):1-9. 10.3345/kjp.2017.60.1.1.

Malformations of cortical development: genetic mechanisms and diagnostic approach

Affiliations
  • 1Department of Pediatrics, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Korea. jhlee0101@skku.edu

Abstract

Malformations of cortical development are rare congenital anomalies of the cerebral cortex, wherein patients present with intractable epilepsy and various degrees of developmental delay. Cases show a spectrum of anomalous cortical formations with diverse anatomic and morphological abnormalities, a variety of genetic causes, and different clinical presentations. Brain magnetic resonance imaging has been of great help in determining the exact morphologies of cortical malformations. The hypothetical mechanisms of malformation include interruptions during the formation of cerebral cortex in the form of viral infection, genetic causes, and vascular events. Recent remarkable developments in genetic analysis methods have improved our understanding of these pathological mechanisms. The present review will discuss normal cortical development, the current proposed malformation classifications, and the diagnostic approach for malformations of cortical development.

Keyword

Malformation; Cerebral cortex; Epilepsy; Developmental delay; Neurogenesis

MeSH Terms

Brain
Cerebral Cortex
Classification
Drug Resistant Epilepsy
Epilepsy
Humans
Magnetic Resonance Imaging
Malformations of Cortical Development*
Neurogenesis
Full Text Links
  • KJP
Actions
Cited
CITED
export Copy
Close
Share
  • Twitter
  • Facebook
Similar articles
Copyright © 2024 by Korean Association of Medical Journal Editors. All rights reserved.     E-mail: koreamed@kamje.or.kr