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. 1989 Aug;82(8):466–469. doi: 10.1177/014107688908200808

Gross and histological criteria for developmental disorders in brains of schizophrenics.

H Jakob 1, H Beckmann 1
PMCID: PMC1292251  PMID: 2674429

Abstract

Autopsy findings and examination of histological sections from 12 schizophrenic patients and from age-matched, non-schizophrenic controls were enlarged and confirmed our previous study. Four subgroups were differentiated with gross abnormalities, in most cases with asymmetry of the temporal sulcal gyral pattern. Two types of macroscopical deviations are described. Different periods of developmental termination, concerning the sulcal gyral pattern of the temporal lobe, suggest a period in which the disturbance of the development originated which coincides with a probably genetically-induced disturbed migration in the entorhinal region toward the end of the fifth month. It is thought that the parahippocampal or entorhinal area develops differently, space- and time-wise. This may explain why migratory disturbances particularly occur in this precisely limited area. The findings in the ventral insular area are discussed, together with factors which also suggest a developmental disorder.

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Selected References

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  1. Bogerts B., Meertz E., Schönfeldt-Bausch R. Basal ganglia and limbic system pathology in schizophrenia. A morphometric study of brain volume and shrinkage. Arch Gen Psychiatry. 1985 Aug;42(8):784–791. doi: 10.1001/archpsyc.1985.01790310046006. [DOI] [PubMed] [Google Scholar]
  2. Brown R., Colter N., Corsellis J. A., Crow T. J., Frith C. D., Jagoe R., Johnstone E. C., Marsh L. Postmortem evidence of structural brain changes in schizophrenia. Differences in brain weight, temporal horn area, and parahippocampal gyrus compared with affective disorder. Arch Gen Psychiatry. 1986 Jan;43(1):36–42. doi: 10.1001/archpsyc.1986.01800010038005. [DOI] [PubMed] [Google Scholar]
  3. Fernández V. An autoradiographic study of the development of the anterior thalamic group and limbic cortex in the rabbit. J Comp Neurol. 1969 Aug;136(4):423–452. doi: 10.1002/cne.901360406. [DOI] [PubMed] [Google Scholar]
  4. Hjorth-Simonsen A. Projection of the lateral part of the entorhinal area to the hippocampus and fascia dentata. J Comp Neurol. 1972 Oct;146(2):219–232. doi: 10.1002/cne.901460206. [DOI] [PubMed] [Google Scholar]
  5. Jakob H., Beckmann H. Prenatal developmental disturbances in the limbic allocortex in schizophrenics. J Neural Transm. 1986;65(3-4):303–326. doi: 10.1007/BF01249090. [DOI] [PubMed] [Google Scholar]
  6. Kovelman J. A., Scheibel A. B. A neurohistological correlate of schizophrenia. Biol Psychiatry. 1984 Dec;19(12):1601–1621. [PubMed] [Google Scholar]
  7. Nowakowski R. S., Rakic P. The site of origin and route and rate of migration of neurons to the hippocampal region of the rhesus monkey. J Comp Neurol. 1981 Feb 10;196(1):129–154. doi: 10.1002/cne.901960110. [DOI] [PubMed] [Google Scholar]
  8. Rakic P. Mode of cell migration to the superficial layers of fetal monkey neocortex. J Comp Neurol. 1972 May;145(1):61–83. doi: 10.1002/cne.901450105. [DOI] [PubMed] [Google Scholar]
  9. Rakic P. Neuronal migration and contact guidance in the primate telencephalon. Postgrad Med J. 1978;54 (Suppl 1):25–40. [PubMed] [Google Scholar]
  10. Rakic P., Nowakowski R. S. The time of origin of neurons in the hippocampal region of the rhesus monkey. J Comp Neurol. 1981 Feb 10;196(1):99–128. doi: 10.1002/cne.901960109. [DOI] [PubMed] [Google Scholar]
  11. Schmechel D. E., Rakic P. Arrested proliferation of radial glial cells during midgestation in rhesus monkey. Nature. 1979 Jan 25;277(5694):303–305. doi: 10.1038/277303a0. [DOI] [PubMed] [Google Scholar]
  12. Segal M., Landis S. Afferents to the hippocampus of the rat studied with the method of retrograde transport of horseradish peroxidase. Brain Res. 1974 Sep 20;78(1):1–15. doi: 10.1016/0006-8993(74)90349-7. [DOI] [PubMed] [Google Scholar]
  13. Shimada M., Abe Y., Yamano T., Ohta S., Yamazaki S., Ohya N. The pathogenesis of abnormal cytoarchitecture in the cerebral cortex and hippocampus of the mouse treated transplacentally with cytosine arabinoside. Acta Neuropathol. 1982;58(3):159–167. doi: 10.1007/BF00690796. [DOI] [PubMed] [Google Scholar]
  14. Stevens J. R., Casanova M. F. Is there a neuropathology of schizophrenia? Biol Psychiatry. 1988 Jun;24(2):123–128. doi: 10.1016/0006-3223(88)90268-5. [DOI] [PubMed] [Google Scholar]

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