Literature DB >> 27670206

Malformations of Cortical Development: From Postnatal to Fetal Imaging.

Tally Lerman-Sagie1, Zvi Leibovitz1.   

Abstract

Abnormal fetal corticogenesis results in malformations of cortical development (MCD). Abnormal cell proliferation leads to microcephaly or megalencephaly, incomplete neuronal migration results in heterotopia and lissencephaly, neuronal overmigration manifests as cobblestone malformations, and anomalous postmigrational cortical organization is responsible for polymicrogyria and focal cortical dysplasias. MCD comprises various congenital brain disorders, caused by different genetic, infectious, or vascular etiologies and is associated with significant neurological morbidity. Although MCD are rarely diagnosed prenatally, both dedicated multiplanar neurosonography and magnetic resonance imaging enable good demonstration of fetal cortical development. The imaging signs of fetal MCD are: delayed or absent cerebral sulcation; premature abnormal sulci; thin and irregular hemispheric parenchyma; wide abnormal overdeveloped gyri; wide opening of isolated sulci; nodular bulging into the lateral ventricles; cortical clefts; intraparenchymal echogenic nodules; and cortical thickening. The postnatal and prenatal imaging features of four main malformations of cortical development-lissencephaly, cobblestone malformations, periventricular nodular heterotopia, and polymicrogyria-are described.

Entities:  

Keywords:  Cobblestone malformation; Lissencephaly; Magnetic resonance imaging; Malformations of cortical development; Periventricular nodular heterotopia; Polymicrogyria; Ultrasound

Mesh:

Year:  2016        PMID: 27670206     DOI: 10.1017/cjn.2016.271

Source DB:  PubMed          Journal:  Can J Neurol Sci        ISSN: 0317-1671            Impact factor:   2.104


  2 in total

1.  Diagnostic value of virtual autopsy using pm-MRI at 3T on malformed second trimester fetuses vs classic autopsy.

Authors:  Adelina Staicu; Camelia Albu; Roxana Popa-Stanila; Cosmina Ioana Bondor; Ioana Cristina Rotar; Florin Stamatian; Daniel Muresan
Journal:  PLoS One       Date:  2021-11-29       Impact factor: 3.240

2.  A prenatal case of lissencephaly with cerebellar hypoplasia: New mutation in RELN gene.

Authors:  Claire Balza; Giulia Garofalo; Teresa Cos; Julie Désir; Xin Kang; Kathelijn Keymolen; Julie Soblet; Kim Van Berkel; Catheline Vilain; Wafa Ben Abbou; Marie Cassart
Journal:  Clin Case Rep       Date:  2021-12-05
  2 in total

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