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