Hostname: page-component-5c6d5d7d68-sv6ng Total loading time: 0 Render date: 2024-09-01T01:27:47.570Z Has data issue: false hasContentIssue false

Lissencephaly

Published online by Cambridge University Press:  18 September 2015

Margaret G. Norman*
Affiliation:
Divisions of Pathology and Genetics, Eleanor M. Paterson Laboratory, Children's Hospital of Eastern Ontario, Ottawa, and Departments of Pathology and Pediatrics, University of Ottawa, Ontario; and Departments of Pathology, Sacre Coeur Hospital, Hull, Quebec and St. Andrews Hospital, Midland, Ontario
Maureen Roberts
Affiliation:
Divisions of Pathology and Genetics, Eleanor M. Paterson Laboratory, Children's Hospital of Eastern Ontario, Ottawa, and Departments of Pathology and Pediatrics, University of Ottawa, Ontario; and Departments of Pathology, Sacre Coeur Hospital, Hull, Quebec and St. Andrews Hospital, Midland, Ontario
J. Sirois
Affiliation:
Divisions of Pathology and Genetics, Eleanor M. Paterson Laboratory, Children's Hospital of Eastern Ontario, Ottawa, and Departments of Pathology and Pediatrics, University of Ottawa, Ontario; and Departments of Pathology, Sacre Coeur Hospital, Hull, Quebec and St. Andrews Hospital, Midland, Ontario
L.J.M. Tremblay
Affiliation:
Divisions of Pathology and Genetics, Eleanor M. Paterson Laboratory, Children's Hospital of Eastern Ontario, Ottawa, and Departments of Pathology and Pediatrics, University of Ottawa, Ontario; and Departments of Pathology, Sacre Coeur Hospital, Hull, Quebec and St. Andrews Hospital, Midland, Ontario
*
Children's Hospital of Eastern Ontario, 401 Smyth Rd. Ottawa, Ont. K1H 8L1 Canada
Rights & Permissions [Opens in a new window]

Summary:

Core share and HTML view are not available for this content. However, as you have access to this content, a full PDF is available via the ‘Save PDF’ action button.

The first reported case of lissencephaly resulting from a consanguinous union strengthens the supposition that in some cases, it is transmitted as an autosomal recessive trait. Comparison of this case with a sporadically occuring case of lissencephaly, with different cortical morphology, suggests that lissencephaly may be an example of either varying gene expressivity or gene-tic heterogeneity. Lissencephaly and pachygyria may eventually be shown to be due to different causes, some inherited, some acquired. The classical examples of lissencephaly are different morphologically from a case in which antenatal cytomegalovirus infection had produced a small smooth brain. This suggests that antenatal viral infections are destructive rather than teratogenic.

Type
Research Article
Copyright
Copyright © Canadian Neurological Sciences Federation 1976

References

REFERENCES

Brun, A., (1965). The subpiai granular layer of the foetal cerebral cortex in man. Acta Pathologica et Microbiologica Scan-dinavica Supplementum 179, 42.Google Scholar
Cowen, D., and Geller, L.M., (1960). Long term pathological effects of prenatal x-irradiation on the central nervous system of the rat. Journal of Neuropathology and Experimental Neurology 19: 488527.CrossRefGoogle ScholarPubMed
Crome, L., (1956). Pachygyria. Journal of Pathology and Bacteriology 30: 335351.CrossRefGoogle Scholar
Crome, L., and France, N.E., (1959). Microgyria and cytomegalic inclusion disease in infancy. Journal of Clinical Pathology 12: 427434.CrossRefGoogle ScholarPubMed
Dambska, M., and Schmidt-SIDOR, B., (1971). Deux cas d’agyrie et son rapport aux malformations du cerveau a l’incidence familiale. Neuropathologia Polska 9: 139144.Google Scholar
Daube, J.R., and Chou, S.M., (1966). Lissencephaly: two cases. Neurology 16: 179191.Google Scholar
Dieker, H., Edwards, R.H., Zu Rhein, G., Chou, S.M., Hartman, H.A., and Opitz, J.M., (1969). The lissencephaly syndrome in Birth defects. Original article series V: 5364.Google Scholar
Hanaway, J., Lee, S.I., and Netsky, M.G., (1968). Pachygyria: relation of findings to modem embryologie concepts. Neurology 18: 791799.CrossRefGoogle Scholar
Holmes, L.B., Driscoll, S., Atkins, L., (1974). Genetic heterogeneity of cebocephaly. Journal of Medical Genetics 11:3540.CrossRefGoogle ScholarPubMed
Hanaway, J., and Netsky, M.G., (1971). Heterotopias of the inferior olive:Relation to Dandy-Walker malformation and correlation with experimental data. Journal of Neuropathology and Experimental Neurology 30: 380389.CrossRefGoogle ScholarPubMed
Harper, I.R., (1967). Infantile spasms associated with cerebral agyria. Developmental Medicine and Child Neurology 9: 460463.CrossRefGoogle ScholarPubMed
Johnson, R.T., (1972). Effects of Viral Infection on the developing nervous system. New England Journal of Medicine 287, 599604.Google ScholarPubMed
Levine, D.N., and Fisher, M.A., Caviness, V.S. Jr., (1974). Porencephaly with microgyria: A pathologic study. Acta Neuropathologica 29: 99113.CrossRefGoogle ScholarPubMed
McKusick, V.A., (1971). Mendelian inheritance in Man: Catalogues of autosomal dominant, autosomal recessives and X-linked phenotypes. p. 440. The Johns Hopkins Press, Baltimore and London.Google Scholar
Miller, J.Q., (1963). Lissencephaly in two siblings. Neurology 13: 841850.CrossRefGoogle Scholar
Navin, J.J., and Angevine, J.M., (1968). Congenital cytomegalic inclusion disease with porencephaly. Neurology 18: 470472.CrossRefGoogle ScholarPubMed
Norman, R.M., (1966). in Greenfields Neuropathology edit Blackwood, W., Mcmenemey, W.H., Meyer, A., Norman, R.M., and Russell, D.S., Baltimore, Williams & Wilkins. p. 384.Google Scholar
Osburn, B.I., Silverstein, A.M., Prendergast, R.A., Johnson, R.T., and Parshall, C.J., (1971). Experimental viral-induced congenital en-cephalopathies I Pathology of hydrence-phaly and porencephaly caused by blue-tongue vaccine virus. Laboratory Investigation 25: 197205.Google ScholarPubMed
Rakic, P., (1972). Mode of cell migration to the superficial layers of fetal monkey neocortex. Journal of Comparative Neurology 145: 6184.CrossRefGoogle Scholar
Reznick, M., Alberca-SERRANO, R., (1964). Forme familiale d’hypertelorisme avec lissencéphalie se présent ant cliniquement sous forme d’une arriération mentale avec epilepsie et paraplégia spasmodic. Journal of Neurological Sciences 1: 4058.CrossRefGoogle Scholar
Rorke, L.B., (1973). Nervous system lesions in the congenital rubella syndrome. Archives of Otolaryngology 98: 249251.CrossRefGoogle ScholarPubMed
Sidman, R.L., and Rakic, P., (1973). Neuronal migration, with special reference to the developing human brain: A review. Brain Research 62: 135.CrossRefGoogle Scholar
Stewart, R.M., Richman, D.P., Caviness, V.S. Jr., (1975). Lissencephaly and pachygyria: An architectonic and topographical analysis. Acta Neuropathologica 31: 112.CrossRefGoogle ScholarPubMed
Williams, R.S., Ferrante, R.J., and Caviness, V.S. Jr., (1975). Neocortical organization in human cerebral malformation: A Golgi study. Abstract. The Society for Neuroscience, New York, N. Y., November, 1975.Google Scholar