Fetal Agenesis of the Corpus Callosum MRI
Midsagittal view directly shows the CC; complete vs partial agenesis; focus on associated anomalies + chromosomes, MRI superior to ultrasound.
Complete agenesis · assess associated anomalies: Complete agenesis: direct (CC not seen on midsagittal) + indirect (colpocephaly, parallel lateral ventricles racing-car/longhorn sign, elev…
Step-by-step decision
Choose step by step as prompted; reaching an endpoint gives the management recommendation. You can go back a step or restart anytime.
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Full pathway
- [Decision] Corpus callosum MRI assessmentCorpus callosum MRI assessment (midsagittal direct visualization)? (The CC develops front-to-back at 10–18/20 weeks (genu first, splenium/rostrum last). MRI is superior to ultrasound (midsagittal directly shows the CC; ultrasound relies on indirect signs like absent cavum septi pellucidi). Suspect a CC anomaly when there is ventriculomegaly.)
- CC normal/equivocal (need to re-check indirect signs) → CC normal
- Partial agenesis/hypoplasia (usually missing splenium/rostrum) → Partial agenesis/hypoplasia
- Complete agenesis (CC not seen at all on midsagittal + indirect signs) → Complete agenesis · assess associated anomalies
- [End] CC normalCC normal: midsagittal shows a complete C-shaped CC, cavum septi pellucidi present; exclude indirect signs (colpocephaly/parallel lateral ventricles); if only equivocal → coronal re-check (distinguish hypoplasia from a normal variant, and ectopic hippocampal commissure).
- [End] Partial agenesis/hypoplasiaPartial agenesis/hypoplasia (usually missing posterior splenium/rostrum): fetal MRI to measure CC length/thickness against gestational age; assess indirect signs (colpocephaly, elevated third ventricle) and associated anomalies; karyotype/microarray; prognosis is slightly better than complete but variable, counseling needed.
- [End] Complete agenesis · assess associated anomaliesComplete agenesis: direct (CC not seen on midsagittal) + indirect (colpocephaly, parallel lateral ventricles racing-car/longhorn sign, elevated third ventricle ± dorsal cyst, absent cavum septi pellucidi, Probst bundles, radial gyri); focus on associated anomalies (interhemispheric cyst, migration/cortical malformation, Dandy-Walker, holoprosencephaly) + karyotype/microarray — isolated complete ACC usually has a fair prognosis but variable; multidisciplinary counseling.
Source guidelines & references
- Fetal corpus callosum anomalies MRI assessment and associated anomalies (Diagnostics 2024; Brain 2024 expert consensus)
This pathway is our own synthesis of the decision logic in the guidelines above (not the guideline verbatim); thresholds and workflows change as guidelines update — in practice follow the latest guideline, your institution's protocol and the individual patient.
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