Chromosomal aberrations and schizophrenia. Autosomes.

作者: Anne S. Bassett

DOI: 10.1192/BJP.161.3.323

关键词: PsychosisGenetic heterogeneitySchizophreniaBiologyGene mappingFamily historyGeneticsAutosomeGenetic linkageCytogenetics

摘要: Chromosomal aberrations associated with schizophrenic disorders may suggest regions in which to focus a search for genes predisposing schizophrenia by linkage strategy. As other genetic illnesses, chromosomal abnormalities also provide useful tools subsequent physical mapping, fine localisation, and isolation of important susceptibility genes. Identification several be especially important, given the unknown pathophysiology, paucity known brain genes, probable heterogeneity manic-depression. However, because psychiatric are common inherited complex manner, researchers must use caution when drawing inferences about associations aberrations. Reported involving autosomes (chromosomes 1-22) psychotic reviewed. Their relevance studies localising was estimated standardised criteria specificity, diagnosis, family history, overall weight evidence. Four 'possibly relevant' were identified: 5q, 11q, 18q, 19p. This paper outlines strategies future detect new major that relevant isolating schizophrenia.

参考文章(71)
Lynn E. Delisi, Michael Lovett, The Role of Molecular Genetics in Psychiatry: Unraveling the Etiology for Schizophrenia Springer, New York, NY. pp. 131- 161 ,(1990) , 10.1007/978-1-4612-3248-3_7
N Risch, Linkage strategies for genetically complex traits. I. Multilocus models. American Journal of Human Genetics. ,vol. 46, pp. 222- 228 ,(1990)
Philip M. Marden, David W. Smith, Michael J. McDonald, Congenital anomalies in the newborninfant, including minor variations The Journal of Pediatrics. ,vol. 64, pp. 357- 371 ,(1964) , 10.1016/S0022-3476(64)80188-8
Digamber S Borgaonkar, Chromosomal variation in man ,(1977)
Kenneth Lyons Jones, Marilyn Crandall Jones, Miguel Del Campo., Smith's recognizable patterns of human malformation Elsevier Saunders. ,(1997)
Grant R. Sutherland, Lisa G. Shaffer, R. J. M. Gardner, Chromosome Abnormalities and Genetic Counseling ,(1989)
J G Hall, Genomic imprinting: review and relevance to human diseases. American Journal of Human Genetics. ,vol. 46, pp. 857- 873 ,(1990)
J. R. Bunzow, David Grandy, H. Makam, O. Civelli, M. Litt, L. Reed, L. Allen, M. Marchionni, R. E. Magenis, The human dopamine D2 receptor gene is located on chromosome 11 at q22-q23 and identifies a TaqI RFLP. American Journal of Human Genetics. ,vol. 45, pp. 778- 785 ,(1989)