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Prenatal MRI detects imaging characteristics in fetuses with complete agenesis of the corpus callosum and associated malformations

Prenatal MRI detects imaging characteristics in fetuses with complete agenesis of the corpus callosu…
Photo by Scott Goodwill / Unsplash
Key Takeaway
Note that prenatal MRI accurately detects associated unilateral hemispheric cortical malformations missed by ultrasound in fetal cACC.

This retrospective cohort study included 101 cases of fetuses diagnosed with complete agenesis of the corpus callosum via prenatal MRI. Sixteen of these cases also had associated unilateral hemispheric cortical malformation. The study setting was not reported, and the follow-up duration was not reported. Safety data regarding adverse events, serious adverse events, discontinuations, and tolerability were not reported.

The fetal gender distribution consisted of 13 male and 3 female cases. Gestational age at diagnosis ranged from 23 weeks to 27 weeks and 2 days. Regarding hemispheric location, the left hemisphere was involved in 7 cases and the right hemisphere in 9 cases. Malformation types included Type I (C1 type) in 11 cases, Type II (C4 type) in 1 case, and Type III (C5 type) in 4 cases. The rake sign and garland sign were observed in all 11 Type I cases. Lobar involvement showed the frontal lobe in 16 cases, the parietal lobe in 10 cases, the occipital lobe in 8 cases, and no temporal lobe involvement.

The primary outcome assessed imaging characteristics and associations with fetal gender and gestational age. No secondary outcomes were reported. The study limitations were not explicitly detailed in the provided data. Funding or conflicts of interest were not reported. The evidence is observational, so causal language is avoided. The practice relevance notes that prenatal MRI is essential for optimizing perinatal management and parental genetic counseling.

Study Details

Study typeCohort
EvidenceLevel 3
PublishedMay 2026
View Original Abstract ↓
IntroductionTo explore the prenatal MRI features of fetal complete agenesis of the corpus callosum (cACC) associated with unilateral hemispheric cortical malformation.MethodsA retrospective analysis was conducted on 101 cases diagnosed with cACC via prenatal MRI. Among them, 16 cases were found to be associated with unilateral hemispheric cortical malformation. The imaging characteristics of this specific malformation were analyzed, and its associations with fetal gender and gestational age were investigated.ResultsIn this group of 16 cases of cACC with unilateral cortical malformation, 13 fetuses were male and 3 were female. The gestational age at diagnosis ranged from 23 weeks to 27 weeks and 2 days. The malformation was located in the left hemisphere in 7 cases and in the right hemisphere in 9 cases. Type I (C1 type: extensive cortical twisting/folding) was observed in 11 cases, all of which exhibited the “rake sign” and “garland sign”. The “rake sign” manifests as abnormally folded dysplastic cortex resembling a rake on axial or coronal views, while the “garland sign” appears as abnormally folded dysplastic cortex resembling a garland on sagittal views. Type II (C4 type: transcortical cleft formation) was observed in 1 case, and Type III (C5 type: focal cortical indentation or serrated changes) was observed in 4 cases. The unilateral cortical malformation involved the frontal lobe in 16 cases, the parietal lobe in 10 cases, and the occipital lobe in 8 cases, with no involvement of the temporal lobe.DiscussionFetal agenesis of the corpus callosum has a relatively high probability of being associated with unilateral cortical malformation. This malformation occurs more frequently in males, is mostly detected during the mid-trimester, and most commonly involves the frontal lobe. The “rake sign” and “garland sign” are its characteristic imaging features. Prenatal definitive diagnosis aids in the perinatal management of this malformation. Prenatal MRI is a crucial supplementary examination for fetal cACC diagnosed by prenatal ultrasound, as it can accurately detect associated unilateral hemispheric cortical malformations that are easily missed by ultrasound, and thus is essential for optimizing perinatal management and parental genetic counseling.
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