Summary
Although rare, complex chromosomal rearrangements have been reported in the literature. The result is multiple congenital malformations in the offspring and recurrent spontaneous abortion. Chromosome 7 is usually involved, but in our patient chromosome 18 was involved.
Similar content being viewed by others
References
Gardner RJM, Monk NA, Allen GJ, Parslow MI (1986) A threeway translocation in mother and daughter. J Med Genet 23:90.
Kausch K, Haaf T, Köhler J, Schmid M (1988) Complex chromosomal rearrangement in a women with multiple miscarriages. Am J Med Genet 31:415–420.
Kleczkowska A, Fryns P, Berghe H van den (1982) Complex chromosome rearrangements (CCR) and their genetic consequences. J Genet Hum 30:199–214.
Kousseff BG, Nichols P, Essig Y, Miller K, Weiss A, Tedesco T (1987) Complex chromosome rearrangement and congenital anomalies. Am J Med Genet 26:771–782.
Walker S, Howard PJ, Hunter D (1985) Familial complex autosomal translocations involving chromosome 7, 8 and 9 exhibiting male and female transmission with segregation and recombination. J Med Genet 22:484–491.
Author information
Authors and Affiliations
Rights and permissions
About this article
Cite this article
Timár, L., Béres, J., Kosztolányi, G. et al. De novo complex chromosomal rearrangement in a woman with recurrent spontaneous abortion and one healthy daughter. Hum Genet 86, 421 (1991). https://doi.org/10.1007/BF00201851
Received:
Revised:
Issue Date:
DOI: https://doi.org/10.1007/BF00201851