Subject 1 |
20 + 2 |
21 + 3 |
No signs of cerebral malformations |
Placental hypoplasia, small for gestational age, coarctation of the aorta |
Subject 2 |
20 + 1 |
22 + 0 |
Joubert syndrome with hypoplastic vermis and molar-tooth configuration of the mesencephalon, heterotopic projection of the pyramidal tract into the interpeduncular cistern with interpeduncular white matter heterotopia and absence of the pyramidal tract caudal to the mesencephalon, normal anatomy of corpus callosum and internal capsule |
Multicystic kidneys |
Subject 3 |
20 + 4 |
22 + 1 |
Complete ACC, abnormal gyri and sulci in both frontal lobes, periventricular and subcortical gray matter heterotopia, malrotation of the right hippocampus, disorganized fiber architecture in the left corona radiata |
No extracranial malformations |
Subject 4 |
22 + 0 |
22 + 4 |
Complete ACC, subependymal heterotopia, hippocampal malrotation, cerebellar hypoplasia |
Hypertelorism |
Subject 5 |
22 + 0 |
23 + 5 |
Complete ACC, abnormal gyri and sulci in both frontal lobes, malformation of the left frontal lobe with disturbed lamination of the telencephalic wall, abnormal white matter architecture, and enlarged ganglionic eminence, midline cyst |
Hypertelorism, epicanthic folds |
Subject 6 |
25 + 1 |
26 + 3 |
No signs of cerebral malformations |
Congenital muscular dystrophy, pulmonary hypoplasia, cardiac dilatation |
Subject 7 |
27 + 1 |
29 + 0 |
Complete ACC, abnormal gyri and sulci in the right frontal lobe, delayed sulcation in the temporal lobes |
Parvovirus infection, no extracranial malformations |