Abstract
A structural abnormality of chromosome 4 [inv 4 (p15.2; q21.3)] is reported in a male presenting with DSM-III-R schizophrenia, undifferentiated type (295.94) and in his mother, who displayed symptoms associated with schizotypal personality disorder (DSM-III-R 301.22). The proband had a performance IQ of 91, poor motor coordination, stature in the lowest quartile and an impaired sense of time. There were no diagnostic physical or neurological abnormalities. Mild ventricular enlargement and prominent sulci were found on computed tomography. Both he and his chromosomally normal father had strabismus which required surgical correction. This case joins the long list of chromosomal abnormalities previously reported to confer an increased risk of mental illness and emphasizes the importance of a sophisticated differential diagnosis in evaluating patients who present with symptoms of schizophrenia. The implications for recent initiatives which attempt to localize genes conferring susceptibility to schizophrenia and other major mental illnesses are discussed.
Full text
PDF







Images in this article
Selected References
These references are in PubMed. This may not be the complete list of references from this article.
- Axelsson R., Wahlström J. Chromosome aberrations in patients with paranoid psychosis. Hereditas. 1984;100(1):29–31. doi: 10.1111/j.1601-5223.1984.tb00100.x. [DOI] [PubMed] [Google Scholar]
- Baccichetti C., Tenconi R., Caufin D., Bortotto L. Study on segregation of the inversion of chromosome 4 (p15.2q11) in two unrelated families. Hum Genet. 1982;62(2):117–120. doi: 10.1007/BF00282297. [DOI] [PubMed] [Google Scholar]
- Bassett A. S. Chromosomal aberrations and schizophrenia. Autosomes. Br J Psychiatry. 1992 Sep;161:323–334. doi: 10.1192/bjp.161.3.323. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Bassett A. S., McGillivray B. C., Jones B. D., Pantzar J. T. Partial trisomy chromosome 5 cosegregating with schizophrenia. Lancet. 1988 Apr 9;1(8589):799–801. doi: 10.1016/s0140-6736(88)91660-1. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Crow T. J. Sex chromosomes and psychosis. The case for a pseudoautosomal locus. Br J Psychiatry. 1988 Nov;153:675–683. doi: 10.1192/bjp.153.5.675. [DOI] [PubMed] [Google Scholar]
- Francke U., Arias D. E., Nyham W. L. Proximal 4p-deletion: phenotype differs from classical 4p-syndrome. J Pediatr. 1977 Feb;90(2):250–252. doi: 10.1016/s0022-3476(77)80642-2. [DOI] [PubMed] [Google Scholar]
- Francke U. Retinoblastoma and chromosome 13. Birth Defects Orig Artic Ser. 1976;12(7):131–134. [PubMed] [Google Scholar]
- GJESSING R., GJESSING L. Some main trends in the clinical aspects of periodic catatonia. Acta Psychiatr Scand. 1961;37:1–13. doi: 10.1111/j.1600-0447.1961.tb06155.x. [DOI] [PubMed] [Google Scholar]
- Greenberg D. A. There is more than one way to collect data for linkage analysis. What a study of epilepsy can tell us about linkage strategy for psychiatric disease. Arch Gen Psychiatry. 1992 Sep;49(9):745–750. doi: 10.1001/archpsyc.1992.01820090073012. [DOI] [PubMed] [Google Scholar]
- KAY D. W. Late paraphrenia and its bearing on the aetiology of schizophrenia. Acta Psychiatr Scand. 1963;39:159–169. doi: 10.1111/j.1600-0447.1963.tb07464.x. [DOI] [PubMed] [Google Scholar]
- McGuffin P., Sargeant M., Hetti G., Tidmarsh S., Whatley S., Marchbanks R. M. Exclusion of a schizophrenia susceptibility gene from the chromosome 5q11-q13 region: new data and a reanalysis of previous reports. Am J Hum Genet. 1990 Sep;47(3):524–535. [PMC free article] [PubMed] [Google Scholar]
- Narahara K., Himoto Y., Yokoyama Y., Kasai R., Hata A., Kikkawa K., Takahashi Y., Wakita Y., Kimura S., Kimoto H. The critical monosomic segment involved in 4p- syndrome: a high-resolution banding study on five inherited cases. Jinrui Idengaku Zasshi. 1984 Dec;29(4):403–413. doi: 10.1007/BF01876498. [DOI] [PubMed] [Google Scholar]
- Owen M. J. Will schizophrenia become a graveyard for molecular geneticists? Psychol Med. 1992 May;22(2):289–293. doi: 10.1017/s0033291700030221. [DOI] [PubMed] [Google Scholar]
- Price W. H., Brunton M., Buckton K., Jacobs P. A. Chromosome survey of new patients admitted to the four maximum security hospitals in the United Kingdom. Clin Genet. 1976 Apr;9(4):389–398. doi: 10.1111/j.1399-0004.1976.tb02268.x. [DOI] [PubMed] [Google Scholar]
- Propping P. Genetic disorders presenting as "schizophrenia". Karl Bonhoeffer's early view of the psychoses in the light of medical genetics. Hum Genet. 1983;65(1):1–10. doi: 10.1007/BF00285021. [DOI] [PubMed] [Google Scholar]
- Riccardi V. M. Von Recklinghausen neurofibromatosis. N Engl J Med. 1981 Dec 31;305(27):1617–1627. doi: 10.1056/NEJM198112313052704. [DOI] [PubMed] [Google Scholar]
- Rivas F., García-Esquivel L., Rivera H., Jiménez M. E., González R. M., Cantú J. M. Inv(4)(p16q21). A five-generation pedigree with 24 carriers and no recombinants. Clin Genet. 1987 Feb;31(2):97–101. doi: 10.1111/j.1399-0004.1987.tb02776.x. [DOI] [PubMed] [Google Scholar]
- SLATER E., BEARD A. W., GLITHERO E. The schizophrenialike psychoses of epilepsy. Br J Psychiatry. 1963 Jan;109:95–150. doi: 10.1192/bjp.109.458.95. [DOI] [PubMed] [Google Scholar]
- Sherrington R., Brynjolfsson J., Petursson H., Potter M., Dudleston K., Barraclough B., Wasmuth J., Dobbs M., Gurling H. Localization of a susceptibility locus for schizophrenia on chromosome 5. Nature. 1988 Nov 10;336(6195):164–167. doi: 10.1038/336164a0. [DOI] [PubMed] [Google Scholar]
- Soukup S. W., Yarema W., Robinow M. A pericentric inversion of a chromosome 4 with a t(4q+10p-) and a familial t(DqDq) in a mentally retarded girl. Humangenetik. 1974;25(1):69–78. doi: 10.1007/BF00281009. [DOI] [PubMed] [Google Scholar]
- St George-Hyslop P. H., Tanzi R. E., Polinsky R. J., Haines J. L., Nee L., Watkins P. C., Myers R. H., Feldman R. G., Pollen D., Drachman D. The genetic defect causing familial Alzheimer's disease maps on chromosome 21. Science. 1987 Feb 20;235(4791):885–890. doi: 10.1126/science.2880399. [DOI] [PubMed] [Google Scholar]
- Tengström C., Autio S. Chromosomal aberrations in 85 mentally retarded patients examined by high resolution banding. Clin Genet. 1987 Jan;31(1):53–60. [PubMed] [Google Scholar]
- Weissenbach J., Gyapay G., Dib C., Vignal A., Morissette J., Millasseau P., Vaysseix G., Lathrop M. A second-generation linkage map of the human genome. Nature. 1992 Oct 29;359(6398):794–801. doi: 10.1038/359794a0. [DOI] [PubMed] [Google Scholar]
- Young R. S., Weaver D. D., Kukolich M. K., Heerema N. A., Palmer C. G., Kawira E. L., Bender H. A. Terminal and interstitial deletions of the long arm of chromosome 7: a review with five new cases. Am J Med Genet. 1984 Feb;17(2):437–450. doi: 10.1002/ajmg.1320170207. [DOI] [PubMed] [Google Scholar]
- Yunis J. J. High resolution of human chromosomes. Science. 1976 Mar 26;191(4233):1268–1270. doi: 10.1126/science.1257746. [DOI] [PubMed] [Google Scholar]

