Fig. 2From: Novel PPP1R21 mutation in a family with autosomal recessive neurodevelopmental disorder: results of genomics and molecular analysisBrain MRI of the patient (right to left sagittal T1, axial T2 and coronal T2 images) showing mild ventricular hypoplasia with prominent CSF spaces, reduced white matter volume, hypoplasia of corpus callosum, and cavum septum pellucidumBack to article page