Skip to main content
Figure 5 | Acta Neuropathologica Communications

Figure 5

From: Mutations in tubulin genes are frequent causes of various foetal malformations of cortical development including microlissencephaly

Figure 5

MRI of LIS_TUB_012 foetus 22 with polymicrogyria-like cortical dysplasia at 36 WG with TUBA1A mutation (p.P72S) showing asymmetrical left predominant perisylvian polymicrogyria on coronal (a,b) and axial (d) T2-weighted sections, the corpus callosum is hypoplastic and thin, and the cerebellum and the brainstem appear to be hypoplastic on sagittal (c) and coronal section (b).

Back to article page

Acta Neuropathologica Communications

ISSN: 2051-5960

Contact us