Abstract
Marriages involving partners both of whom have abnormal karyotypes are rare and are usually ascertained because of a history of infertility, repeated abortions, or the birth of a balanced translocation carrier or chromosomally abnormal offspring. Abnormalities which have been noted include sex chromosome aberrations in both parents or a sex chromosome abnormality in one parent and an autosomal abnormality in the other. Four papers have reported balanced reciprocal autosomal translocations in both parents, two couples representing a first cousin marriage. We present a case of a paternal 13;14 Robertsonian translocation and a maternal (7p;13q) reciprocal translocation in a couple with repeated fetal loss.
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.
- Buhler E. M., Kosztolanyi G., Stalder G. R. Letter: Possible mosaic XXX-XXY marriage with abnormal offspring. Lancet. 1975 Feb 8;1(7902):334–334. doi: 10.1016/s0140-6736(75)91241-6. [DOI] [PubMed] [Google Scholar]
- Chandley A. C., Christie S., Fletcher J., Frackiewicz A., Jacobs P. A. Translocation heterozygosity and associated subfertility in man. Cytogenetics. 1972;11(6):516–533. doi: 10.1159/000130218. [DOI] [PubMed] [Google Scholar]
- Dallapiccola B., Chessa L., Brinchi V., Frontali M., Gandini E. Mating between two balanced translocation carriers in two unrelated families. Hum Genet. 1983;65(2):165–168. doi: 10.1007/BF00286655. [DOI] [PubMed] [Google Scholar]
- Fraccaro M., Maraschio P., Pasquali F., Tiepolo L., Zuffardi O., Giarola A. Male infertility and 13-14 translocation. Lancet. 1973 Mar 3;1(7801):488–488. doi: 10.1016/s0140-6736(73)91916-8. [DOI] [PubMed] [Google Scholar]
- Harris D. J., Hankins L., Begleiter M. L. Reproductive risk of t(13q14q) carriers: case report and review. Am J Med Genet. 1979;3(2):175–181. doi: 10.1002/ajmg.1320030208. [DOI] [PubMed] [Google Scholar]
- Mulcahy M. T., Watson M. Prenatal diagnosis of a double heterozygote for two reciprocal translocations of familial origin. Prenat Diagn. 1983 Oct;3(4):351–353. doi: 10.1002/pd.1970030413. [DOI] [PubMed] [Google Scholar]
- Simoni G., Dalprà L., Terzoli G. L., Rossella F., Tibiletti M. G. The offspring of marriage between two first cousins with the same reciprocal translocation t(2;7)(p11;q31). Hum Genet. 1980;55(2):199–202. doi: 10.1007/BF00291767. [DOI] [PubMed] [Google Scholar]
- Utility and limitations of chromosome banding in pre- and postnatal service cytogenetics. Am J Med Genet. 1981;9(1):86–87. doi: 10.1002/ajmg.1320090115. [DOI] [PubMed] [Google Scholar]
- de Grouchy J., Finaz C., Roubin M., Roy J. Deux translocations familiales survenues ensemble chez chacune de deuc soeurs, l'une équilibrée, l'autre trisomique partielle 10q. Ann Genet. 1972 Jun;15(2):85–92. [PubMed] [Google Scholar]


