Abstract
The first case of a liveborn male infant trisomic for both the X and the No 18 chromosome is presented. The patient had multiple congenital anomalies many of which were similar in appearance to patients with trisomy 18. The proband died after 2 days. Both maternal and paternal karyotypes were normal.
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- Bach C., Toublanc J. E., Gautier M. Une observation de double aneupoïdie chromosomique: trisomie 18 et XX. Ann Genet. 1973 Mar;16(1):61–66. [PubMed] [Google Scholar]
- Cohen M. M., Bumbalo T. S. Double aneuploidy: trisomy-18 and Klinefelter's syndrome. Am J Dis Child. 1967 Apr;113(4):483–486. doi: 10.1001/archpedi.1967.02090190129017. [DOI] [PubMed] [Google Scholar]
- Madahar D. P., Dosik H., Wexler I. 48,XXX, plus 18 double trisomy. J Med Genet. 1974 Sep;11(3):309–311. doi: 10.1136/jmg.11.3.309. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Malhes J. B., Moore C. M., Gershank J. J. A case of double trisomy in a liveborn infant: 48, XXY, "13. Clin Genet. 1977 Feb;11(2):147–150. doi: 10.1111/j.1399-0004.1977.tb01292.x. [DOI] [PubMed] [Google Scholar]
- Nielsen J., Vetner M., Holm V., Askjaer A. S., Reske-Nielsen E., Zizka J. Klinefelter's syndrome and trisomy 18 in a newborn boy. Clin Genet. 1978 Mar;13(3):259–264. doi: 10.1111/j.1399-0004.1978.tb01179.x. [DOI] [PubMed] [Google Scholar]