Introduction
Malformations of cortical development (MCD) comprise myriad disorders related to disruption of the complex process of cortex formation, caused by various genetic, infectious, or vascular etiologies. MCD are associated with significant neurological morbidity, including intellectual disability, epilepsy, and motor dysfunction.Reference Leventer, Phelan, Coleman, Kean, Jackson and Harvey 1
The discovery of chromosome 17p13.3 deletions, followed by mutations in LIS1, in children with lissencephaly in 1983, marked the beginning of a new era of understanding the genetic basis and the pathogenesis of brain malformations.Reference Dobyns, Stratton, Parke, Greenberg, Nussbaum and Ledbetter 2
Since then, the accelerated rate of gene discovery, particularly with the introduction of next-generation sequencing (NGS), has uncovered a large number of novel genes associated with malformations of cortical development.Reference Mirzaa and Paciorkowski 3
Although early embryonic malformations of dorsal and ventral induction (including cephalic neural tube defects and holoprosencephaly) are frequently associated with an anomalous cerebral cortex, the MCD are related to later events in fetal corticogenesis that are controlled by three overlapping developmental stages: neural stem cell proliferation, migration, and organization. Abnormal cell proliferation may cause primary microcephaly, megalencephaly, or hemimegalencephaly. Failure of initial neuronal migration results in periventricular heterotopia. Disorders of later migration cause disruption of the normal six-layered cortex (classical lissencephaly) and subcortical band heterotopia; however, neurons that fail to stop at their intended cortical destination and continue to migrate onto the cortical surface result in cobblestone malformation. Finally, abnormal postmigrational development underlies polymicrogyria (PMG) and focal cortical dysplasias. Because of the overlap between the developmental stages, disorders of corticogenesis may present with complex cortical malformations.Reference Barkovich, Guerrini, Kuzniecky, Jackson and Dobyns 4
The diagnosis of MCD requires high-resolution multiplanar magnetic resonance imaging because of its ability to demonstrate excellent contrast resolution between white matter and gray matter, to characterize topographically the development of cortical gyri and sulci, and to analyze accurately the formation of white matter and stages of myelination.Reference Andrade and Leite Cda 5
MCD are rarely diagnosed prenatally. This can be explained by the late gestational appearance of their typical morphological features, usually beyond the recommended time of the routine fetal anatomical sonographic scan (19-23 weeks). Moreover, the low antenatal MCD detection rate may be related to the common standards of basic fetal brain ultrasound imaging, restricted to the axial planes at the level of the lateral ventricles, thalami, third ventricle, cavum septi pellucidi , cerebellum, and cisterna magna.Reference Malinger, Lev and Lerman-Sagie 6 Performance of ultrasonography only in the axial plane may lead to misdiagnosis of MCD that are evident only in the coronal and sagittal planes; however, both dedicated neurosonography and fetal magnetic resonance imaging (MRI) are able to accurately depict fetal cortical malformations, and many articles have been published in the past decade describing these achievements.
Sonography is the most important imaging method for prenatal malformation screening because it is noninvasive, widely available, and safe for both mother and fetus. The ultrasonographic approach to evaluating the fetal brain is based on the classic transabdominal visualization of three different axial planes: the transventricular, the transthalamic, and the transcerebellar (not sufficient for optimal depiction of malformations of the cortex and midline brain structures), supplemented by a more comprehensive, multiplanar approach, in which coronal and sagittal planes are added to the axial ones by a transvaginal or transabdominal scan.Reference Malinger, Kidron and Schreiber 7
MRI was introduced into fetal imaging more than 30 years ago and is a valuable complementary tool in the imaging of structural anomalies of the fetal brain.
Implementation of fast and ultrafast sequences has allowed reduction of acquisition time, which has subsequently decreased artifacts resulting from fetal movements. Fetal MRI has higher contrast resolution than prenatal sonography and enables better differentiation of normal from abnormal tissue.Reference Guibaud 8 , Reference Sonigo, Rypens and Carteret 9
Fetal MRI is performed primarily using ultrafast MRI techniques known as single-shot, fast spin-echo or half-Fourier acquired single-shot turbo spin-echo. Using these rapid-pulse sequences, a single T2-weighted image can be acquired in less than 1 second, reducing the likelihood of fetal motion during image acquisition.Reference Malinger, Kidron and Schreiber 7 , Reference Guibaud 8 When the fetal brain is being evaluated, images are obtained with a section thickness of 3 mm with no gap, in axial, sagittal, and coronal planes.Reference Guibaud 8 - Reference Glenn and Barkovich 11
With the recent application of advanced MRI techniques, an opportunity to investigate the developing brain is available beyond the qualitative morphologic evaluation.Reference Limperopoulos and Clouchoux 12 , Reference Glenn 13
The earliest recognition of MCD is reported at the 22nd week of gestation in fetuses with Miller-Dicker and Walker-Warburg syndrome by demonstration of abnormal formation of the Sylvian fissures,Reference Fong, Ghai and Toi 14 which is enabled by the knowledge of their normal imaging pattern of development (Figure 1A-C).Reference Chen, Zimmerman and Faro 15 - Reference Lerman-Sagie and Malinger 18
Figure 1 Normal and abnormal development of the operculum at 23 gestational weeks (transabdominal ultrasound in the axial plane). (A) Normal; note the square-shaped operculum. (B) Lissencephaly; note the minimal opercular indentation. (C) Generalized PMG; note the shallow irregular opercular shape.
Delayed or absent cerebral sulcation is considered a principal feature of fetal MCD. Several additional indicative sonographic signs have been described: premature abnormal sulci; thin and irregular cortical mantle; wide abnormal overdeveloped gyri; wide opening of isolated sulci; nodular bulging into the lateral ventricles; cortical clefts; and intraparenchymal echogenic nodules.Reference Malinger, Lev and Lerman-Sagie 6 , Reference Malinger, Kidron and Schreiber 7 , Reference Malinger, Lev and Lerman-Sagie 19
In late gestational weeks, the diagnosis of MCD by MRI is more accurate than by ultrasound, primarily because of brain sonographic shadowing caused by the skull bones and technical difficulties in attaining an appropriate acoustic window. MRI can add information and clarify the different gyration patterns that can be difficult to discern by ultrasound.Reference Blondiaux and Garel 20
The MRI signs suggestive of MCD are similar to ultrasound and include: delayed cortical development; dysgenesis of the Sylvian fissure; delayed sulcal appearance; cortical thickening; irregularity of the ventricular wall; absence or abnormal appearance of fissures; abnormal, asymmetric gyri; and discontinuous cortex.Reference Fong, Ghai and Toi 14 , Reference Guibaud, Selleret and Larroche 21
Because MCD were initially depicted in children, in this article, we first describe the postnatal imaging features, and then the etiology (genetic or disruptive) followed by the fetal sonographic and MRI findings. We demonstrate four main malformations of cortical development: lissencephaly, cobblestone malformations, periventricular nodular heterotopia, and PMG.
Lissencephaly Type I
Lissencephaly is defined as a smooth brain and characterized by abnormalities in the width of the gyri and the thickness of the cortex. The neocortex of lissencephalic patients lacks normal cortical lamination and contains two to four layers instead of six.Reference Guerrini and Dobyns 22 Classic or type 1 lissencephaly appears as complete or incomplete agyria. The degree of agyria is graded. The complete form is characterized by a smooth surface of the entire brain. In the incomplete form, which is the more commonly seen type, there is a gradient of severity either anterior to posterior or posterior to anterior depending on the genetic defect.
The important postnatal MRI findings of classical lissencephaly are: a hourglass configuration of the brain with large ventricles in the complete form; a thick, smooth thickened cortex (>10 mm) separated from a deep layer of neurons by a “cell sparse layer”; thin subcortical white matter; lack of gray-white matter interdigitations; and shallow Sylvian fissures (Figure 2E,F).Reference Leventer, Phelan, Coleman, Kean, Jackson and Harvey 1 , Reference Abdel Razek, Kandell, Elsorogy, Elmongy and Basett 23 Lissencephaly is usually symmetric. Agenesis of the corpus callosum or cerebellar hypoplasia can be associated findings depending on the affected gene. The known genes are: LIS1, ARX, RELN, VLDLR, ACTB, ACTG1, DCX, DYNC1H1, KIF2A, TUBA1A, TUBB2B, and TUBG1.Reference Guerrini and Dobyns 22
Figure 2 Lissencephaly type I, prenatal and postnatal imaging (three different cases). (A, B) Ultrasound images (axial and coronal) at 23.5 weeks’ gestation. Note the nearly complete absence of the Sylvian fissures. (C, D) MRI (axial and coronal) at 33 weeks’ gestation. Note thick featureless cortex, “figure of eight” brain configuration, and agenesis of the corpus callosum. (E, F) MRI (axial and coronal) at 1 year of age. Note wide gyri with thick cortex, decreased interdigitation of the white matter, and a posterior-to-anterior gradient (patient with a LIS1 mutation).
Prenatal Diagnosis
Lissencephaly type 1 and Miller-Dieker syndrome are usually diagnosed in utero after 27 to 30 weeks’ gestation, either by detailed neurosonography or MRI, by demonstrated lack of development of the primary sulci that should already be present. Mild ventriculomegaly and delayed opercular development are the earliest signs and can be depicted by 23 weeks of gestation in fetuses at risk.Reference Malinger, Lev and Lerman-Sagie 6 Lissencephaly is diagnosed by demonstration of dysgenesis of the Sylvian fissure, delayed sulcal appearance, callosal abnormality, and cortical thickening (Figure 2A-D).Reference Saltzman, Krauss and Goldman 24 , Reference Greco, Resta and Vimercati 25 Sometimes, zones of normal cortex and zones of pachygyric or agyric cortex alternate. The abnormal opercular formation is responsible for a “figure-eight” shaped brain.Reference Fong, Ghai and Toi 14 Sometimes, the genetic defect can be suspected based on the gradient of the anomaly (anterior > posterior-DCX or posterior > anterior-LIS1), the fetal gender (male-DCX, ARX), associated brain anomalies (agenesis of corpus callosum-ARX, cerebellar hypoplasia-RELN, and abnormal basal ganglia-TUBA1A).
Cobblestone Malformation
Cobblestone malformation, formerly called type 2 lissencephaly, is characterized by a nodular cortical surface accompanied by ocular anomalies and congenital muscular disorders.Reference Abdel Razek, Kandell, Elsorogy, Elmongy and Basett 23 Cobblestone malformations have been divided into three different groups based on severity, with Walker-Warburg syndrome being the most severe form, Fukuyama congenital muscular dystrophy the mildest form, and muscle-eye brain disease being the moderate form. Congenital muscular dystrophy is a key feature.
The structural abnormalities result from lack of connection of the radial glia to the pial limiting membrane and neuronal overmigration through pial gaps.Reference Barkovich, Guerrini, Kuzniecky, Jackson and Dobyns 4
There are many different MRI appearances: posterior pachygyria/agyria, anterior PMG-like appearance, cerebellar dysplasia/cysts, and delayed/absent myelination in central regions. It is associated with fused colliculi, a small pons, a dysmorphic mesencephalon, a dorsal pontomedullary kink, vermian hypogenesis, and cerebellar hypoplasia. Microphthalmia and retinal dysplasia (small and dysplastic globe) are commonly seen as are hydrocephalus and posterior cephalocele.Reference Andrade and Leite Cda 5 , Reference Guerrini and Dobyns 22 , Reference Abdel Razek, Kandell, Elsorogy, Elmongy and Basett 23 Some have associated anomalies of the corpus callosum and septum pellucidum (Figure 3G-I).
Figure 3 Cobblestone malformation, prenatal and postnatal imaging (three different cases). (A-C) Ultrasound images at 26 gestational weeks (sagittal, coronal, and axial). Note severe ventriculomegaly, absence of the Sylvian fissures, no primary sulcation, “Z”-shaped (kinked) brainstem (arrow), and hypoplastic vermis (arrowhead). (D-F) Fetal MRI, sagittal, coronal, and axial images at 34 weeks demonstrate “Z”-shaped (kinked) brainstem (arrow), hypoplastic vermis (arrowhead), severe ventricular dilatation, and abnormal sulcation with thin cortex (courtesy of Dr. Chen Hoffman). (G-I) Neonatal MRI, sequential axial images. Note triventricular hydrocephalus, thick irregular cortex with a cobblestone appearance, increased T2 signal from white matter with no interdigitation, retinal detachment, phthisis bulbi of the right eye, and posterior encephalocele. (In addition, small intraventricular blood clots in G and H).
The currently known genes are: FKTN, POMT1, POMT2, POMGnT1, FKRP, LARGE, and GPR56.Reference Mirzaa and Paciorkowski 3
Prenatal Diagnosis
The prenatal diagnosis of Walker-Warburg syndrome has been reported in families at risk.Reference Crowe, Jassani and Dickerman 26 , Reference Rodgers, Vanner and Pai 27 An early diagnosis in the first trimester may be made if there is a cephalocele.Reference Crowe, Jassani and Dickerman 26 Other suggestive findings are early enlargement of the lateral ventricles, abnormal vermis, retinal detachment,Reference Farrell, Toi and Leadman 28 cataract, abnormal sulcation,Reference Monteagudo, Alayón and Mayberry 29 kinked brainstem, and bifid pons (Figure 3A-F).Reference Monteagudo, Alayón and Mayberry 29 - Reference Strigini, Valleriani and Cecchi 32
Periventricular Nodular Heterotopia
Heterotopia occurs when neurons originating in the periventricular region fail to migrate, leaving tracks or nodules of normal neurons in abnormal locations adjacent to the ependymal lining or in subcortical topography.Reference Andrade and Leite Cda 5 Based on MRI scans, there are three types of heterotopia: periventricular nodular heterotopia, focal subcortical heterotopia, and band heterotopia. Patients usually present with seizures and developmental delay.
Periventricular (subependymal nodular) heterotopias (PNH) are often bilateral and placed adjacent to the walls of the lateral ventricles, frequently in the peritrigonal regions, the temporal and occipital horns.Reference Abdel Razek, Kandell, Elsorogy, Elmongy and Basett 23 The characteristic appearance of nodular heterotopia is small, round- or oval-shaped nodules, isointense with gray matter, located in the subependymal layer and projecting into the ventricular lumen (Figure 4C).
Figure 4 Periventricular nodular heterotopia, prenatal and postnatal imaging. (A) Ultrasound axial image at 32 gestational weeks. (B) MRI of the same fetus at 33 weeks. Note nodular bulging into the ventricles (arrows). (C) Adult MRI (axial image) showing classical periventricular nodular heterotopia (arrows) with a “string of pearls” appearance.
PNH can be unilateral, bilateral, symmetric, asymmetric, anterior, central, posterior, inferior, “string of pearls,” contiguous, multinodular, laminar, or “ribbon like.” Posterior PNH have a significantly higher incidence of associated hippocampal, cerebellar, and brain stem anomalies compared with anterior or diffuse PNH. Diffuse PNH have associated agenesis of the corpus callosum and mega cisterna magna.Reference Abdel Razek, Kandell, Elsorogy, Elmongy and Basett 23
Injury to, or denudation of, the neuroependyma is an important factor in the formation of periventricular nodular heterotopia, rather than a cell-intrinsic motility defect.Reference Barkovich, Guerrini, Kuzniecky, Jackson and Dobyns 4
Genetic etiology is not assigned in most cases. Two loci have been identified: X-linked PNH results from mutations in the filamin A gene (FLNA), and a rare autosomal recessive disorder of PNH with microcephaly results from mutations in ARFGEF2. The majority of familial cases are the result of an alteration in FLNA, in contrast to sporadic PNH cases, in which only 20% to 24% have been identified with a mutation in this gene. PNH can be associated with microdeletion syndromes.Reference van Kogelenberg, Ghedia and McGillivray 33
Prenatal Diagnosis
PNH should be considered in utero when ultrasound depicts an irregular lateral ventricular wall with indentations of periventricular tissue (Figure 4A). The sonographic diagnosis is difficult, particularly when the lateral ventricle width is normal. MRI demonstrates multiple small nodular subependymal foci of low signal intensity, isointense to the germinal matrix, similar to that of the gray matter, located in the margins of the lateral ventricles (Figure 4B). They cannot be distinguished reliably from the subependymal nodules seen in tuberous sclerosis; therefore, it is important to search for other manifestations of tuberous sclerosis, such as cortical hamartomas and cardiac rhabdomyomas. A mega cisterna magna, which can be seen in females with filamin A mutations, may be the initial abnormality and, in association with diffuse periventricular nodules with a string of pearls appearance, may suggest the prenatal diagnosis of FLNA muations.Reference Teixeira, Blondiaux and Cassart 34 - Reference Bargallo, Puerto and De Juan 36 In these cases, it is mandatory to obtain a maternal MRI scan that can demonstrate similar findings. Heterotopia may not be recognized when the nodules are single or small.
Polymicrogyria
Bielschowsky first used the term “polymicrogyria” in 1916 to describe a cerebral or cerebellar cortex with multiple excessive small convolutions. PMG is caused by an interruption in normal cerebral cortical development in the late neuronal migration or early postmigrational development periods.Reference Barkovich, Guerrini, Kuzniecky, Jackson and Dobyns 4 It is not a single entity, but a spectrum of cortical malformations with the common feature being excessive gyration.Reference Stutterd and Leventer 37 All have in common a derangement of the normal six-layered lamination of the cortex, an associated derangement of sulcation, and fusion of the molecular layer across sulci.Reference Barkovich 38
The wide spectrum of PMG disorders has different causes, gross appearance, association with various accompanying malformations or disruptions, and microscopic appearance, making it difficult to understand and properly classify. It has been classified mainly according to imaging patterns.Reference Barkovich 38 , Reference Leventer, Jansen and Pilz 39 There is overlap between true PMG and other disorders with a similar imaging appearance such as the cobblestone malformations.
PMG affects variable portions of the cerebral cortex: it may be focal, multifocal, or diffuse; it may be unilateral, bilateral, and asymmetrical; or bilateral and symmetrical. The most common location (in 60% to 70% of cases) is around the Sylvian fissure, particularly the posterior aspect of the fissure; however, any part of the cerebral cortex, including the frontal, occipital, and temporal lobes, can be affected. PMG may be an isolated malformation or it may be associated with other brain malformations.Reference Barkovich 38
MRI shows excessive cortical gyration with an aspect of cortical thickening and shallow sulci and irregularity of the gray-white matter interface. In cases of the perisylvian syndrome, there is PMG surrounding the operculum with enlarged and vertically oriented Sylvian fissures, extending to the parietal lobes (Figure 5E-G).Reference Andrade and Leite Cda 5
Figure 5 Generalized polymicrogyria in patients with DiGeorge syndrome. (A, B) Ultrasound images (coronal and axial) at 32 weeks’ gestation. Note open, dysmorphic operculum with irregular cortical surface (arrows) facing enlarged perisylvian subarachnoid space. CSP, cavum septi pellucidi. (C, D) MRI scans of the same fetus (coronal and axial) at 33 weeks’ gestation. Note diffuse bilateral polymicrogyria, open dysmorphic opercula (arrows), and lean brain parenchyma with abundant cerebrospinal (CSF) spaces around the hemispheres. (E-G) Neonatal MRI images (E, parasagittal; F-G, axial). Note generalized polymicrogyria, open dysmorphic opercula (arrows), and expanded periopercular CSF spaces.
The etiology of PMG includes: congenital infection (particularly cytomegalovirus infection, localized or diffuse in utero ischemia, or genetic disorders). The known genes include: SRPX2, TBR2, ARFGEF2, NDE1, WDR62, PAX6, KIAA1279, RAB3GAP1, RAB3GAP2, TUBA1A, TUBB2B, TUB3, TUBA8, TUBB5, FOXP2, and RTTN.Reference Mirzaa and Paciorkowski 3
Prenatal Diagnosis
The cortical changes of PMG take place late in pregnancy and appear as localized and/or generalized absence of normal sulcation with multiple abnormal infoldings of the affected cortex.Reference Guibaud 8 In young fetuses (younger than 24 weeks), the identification of this cortical malformation is quite difficult and the manifestations on both ultrasound and MRI are subtle. They include presence of sulci that are not expected according to the gestational age; abnormal opercular development (Figure 1C); an irregular surface of the brain; and absence of the normal signal of the cortical ribbon. Late in pregnancy, the MRI features are similar to what is known in the postnatal period: packed and serrated microgyri, irregular gray-white matter junction, and an aberrant and asymmetrical sulcal pattern.Reference Fogliarini, Chaumoitre and Chapon 40 The most frequent MRI presentation diagnosed in utero demonstrates mild ventricular dilatation associated with numerous sulci in the perisylvian area, with irregular cortex–white matter junction and a prominent subarachnoid space overlying the cortical malformation (Figure 5A-D). Because the MRI pattern of PMG changes with increasing gestational age, it is important to follow young fetuses at risk and repeat the ultrasound and MRI examinations to confirm the diagnosis. The most common cause of fetal PMG is congenital CMV infection. In these cases, PMG is associated with other signs of brain infection such as: ventriculomegaly, abnormal ventricular lining and adhesions, periventricular pseudocysts, temporal cysts, abnormal echogenicity of the white matter, calcifications, and cerebellar anomalies.
In summary, fetal MCD will probably remain rarely diagnosed in the general population because of the currently recommended routine fetal sonographic screening programs, which are not aimed at late gestational dedicated central nervous system examination. However, as demonstrated in our article, knowledge of the normal fetal cortical developmental landmarks and awareness of the indicative sonographic signs of MCD enable prenatal diagnosis. The prenatal features of MCD are delayed or absent cerebral sulcation; premature abnormal sulci; thin and irregular hemispheric parenchyma; abnormal overdeveloped gyri; wide opening of isolated sulci; nodular bulging into the lateral ventricles; cortical clefts; and intraparenchymal nodules.
Disclosures
The authors have nothing to disclose.
