Abstract
Malformations of cortical development are common causes of developmental delay and epilepsy. Some patients have early, severe neurological impairment, but others have epilepsy or unexpected deficits that are detectable only by screening. The rapid evolution of molecular biology, genetics, and imaging has resulted in a substantial increase in knowledge about the development of the cerebral cortex and the number and types of malformations reported. Genetic studies have identified several genes that might disrupt each of the main stages of cell proliferation and specification, neuronal migration, and late cortical organisation. Many of these malformations are caused by de-novo dominant or X-linked mutations occurring in sporadic cases. Genetic testing needs accurate assessment of imaging features, and familial distribution, if any, and can be straightforward in some disorders but requires a complex diagnostic algorithm in others. Because of substantial genotypic and phenotypic heterogeneity for most of these genes, a comprehensive analysis of clinical, imaging, and genetic data is needed to properly define these disorders. Exome sequencing and high-field MRI are rapidly modifying the classification of these disorders.
| Original language | English (US) |
|---|---|
| Pages (from-to) | 710-726 |
| Number of pages | 17 |
| Journal | The Lancet Neurology |
| Volume | 13 |
| Issue number | 7 |
| DOIs | |
| State | Published - Jul 2014 |
| Externally published | Yes |
Bibliographical note
Funding Information:We thank Valerio Conti (Neurogenetics Laboratory, Neuroscience Department, Children's Hospital A Meyer-University of Florence, Florence, Italy) for preparing figures 3 and 4 . This work was supported by the European Union Seventh Framework Programme FP7/2007–2013 under the project DESIRE ( grant agreement number 602531 ) to RG.