Fig. 1From: Novel frameshift mutation in LIS1 gene is a probable cause of lissencephaly: a case reportMRI results. A Volumetric T1 brain MRI axial and B Sagittal planes show a diffuse lissencephaly-pachygyria spectrum predominantly in the posterior areas methylation study for Angelman syndrome was normal and the sequencing of ARX and MECP2 showed no pathogenic mutationsBack to article page