Case contributed by Stacy Goergen
Diagnosis certain


Severe ventriculomegaly.

Patient Data

Age: 25w GA
Gender: Female

1. Severe ventriculomegaly involving lateral ventricles; third ventricle also dilated.

2. Septum pellucidum is absent. This is most likely secondary to perforation due to aqueduct obstruction, rather than primary malformation, as there is dip between the frontal horns (as opposed to the flat roof characteristic of primary failure of septal formation). 

3. Abnormally thin corpus callosum and almost completely absent splenium, consistent with hypoplasia. The degree of VM is not sufficient to account for this purely on the basis of stretching by dilated ventricles, as is seen in simple aqueduct stenosis.

4. Failure of appropriate progression of sulcal development. Primary sulcal development is currently about 4 weeks delayed with only slight concavity seen at the expected locaton of the Sylvian fissure. While underdeveloped opercularisation may be seen in association with aqueduct stenosis alone, and is due to severe VM in that situation, association with enlarged ganglionic eminences is indicative of a malformative cause, and in particular the lissencephalies. The parietooccipital and calcarine sulci are also absent but may be delayed or effaced by simple obstructive ventricular enlargement. 

5. Severely reduced cerebellar biometry consistent with cerebellar hypoplasia.

6. No brainstem kink in this case.

Annotated image

Annotation of key findings.

Confirmed pathogenic TUB1A mutation fitting with the phenotype

Case Discussion

Enlarged ganglionic eminences, thin corpus callosum and cerebellar hypoplasia are key to the diagnosis of fetal tubulinopathy, and should prompt the search for TUBB mutation. 

Note that there is no brainstem kinking in this case. This is a useful sign when present but absence does not exclude the diagnosis of tubulinopathy, 

How to use cases

You can use Radiopaedia cases in a variety of ways to help you learn and teach.

Creating your own cases is easy.