“…The current interest in cytoarchitectural abnormalities is mainly driven by the neurodevelopmental theory: If schizophrenia is not characterized by massive cell loss and significant gliosis in the adult brain (as suggested by most of the studies), the "schizophrenia lesion" might be acquired early in development, could be more subtle, and could involve qualitative alterations of cell shape, cell position, connectivity, and the normally asymmetric development of gyri and fissures in both hemispheres. Most of the cytoarchitectural findings are reported for the limbic and paralimbic structures of the temporal lobe (see Dwork 1997, this issue), but abnormalities of the superior temporal gyrus (Southard 1915;Barta et al 1990;Shenton et al 1992;Falkai et al 1995) and displacement of NADPH-d-positive cortical neurons to the underlying white matter (Akbarian et al 1993a, 19936) are two important findings in the isocortex of schizophrenia patients that need to be replicated. The challenge of this approach is the question "What is normal?…”