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Genetics and mechanisms leading to human cortical malformations

Delfina Romero 1 Nadia Bahi-Buisson 2 Fiona Francis 1, *
* Corresponding author
2 Plateforme de génomique [SFR Necker]
SFR Necker - UMS 3633 / US24 - Structure Fédérative de Recherche Necker
Abstract : Cerebral cortical development involves a complex series of highly regulated steps to generate the laminated structure of the adult neocortex. Neuronal migration is a key part of this process. We provide here a detailed review of cortical malformations thought to be linked to abnormal neuronal migration. We have focused on providing updated views related to perturbed mechanisms based on the wealth of genetic information currently available, as well as the study of mutant genes in animal models. We discuss mainly type 1 lissencephaly, periventricular heterotopia, type II lissencephaly and polymicrogyria. We also discuss functional classifications such as the tubulinopathies, and emphasize how modern genetics is revealing genes mutated in atypical cases, as well as unexpected genes for classical cases. A role in neuronal migration is revealed for many mutant genes, although progenitor abnormalities also predominate, depending on the disorder. We finish by describing the advantages of human in vitro cell culture models, to examine human-specific cells and transcripts, and further mention non-genetic mechanisms leading to cortical malformations.
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Submitted on : Monday, October 30, 2017 - 2:44:41 PM
Last modification on : Friday, March 27, 2020 - 2:50:38 AM
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Delfina Romero, Nadia Bahi-Buisson, Fiona Francis. Genetics and mechanisms leading to human cortical malformations. Seminars in Cell and Developmental Biology, Elsevier, 2017, ⟨10.1016/j.semcdb.2017.09.031⟩. ⟨hal-01626222⟩



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