In six of them, atrophy was associated to unilateral (Pt1, Pt3, Pt6 and Pt7) (Figure 3) or bilateral (Pt2 and Pt10) hippocampal sclerosis, while in two subjects (Pt7 and Pt8), it was associated to lobe temporal hypoplasia. The gene discussed is ZNF135; the disease is Atrophy.