Genetic amniocentesis in twin pregnancies
Article first published online: 19 AUG 2005
DOI: 10.1111/j.1471-0528.1988.tb06599.x
Issue
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BJOG: An International Journal of Obstetrics & Gynaecology
Volume 95, Issue 4, pages 323–326, April 1988
Additional Information
How to Cite
PIJPERS, L., JAHODA, M. G. J., VOSTERS, R. P. L., NIERMEIJER, M. F. and SACHS, E. S. (1988), Genetic amniocentesis in twin pregnancies. BJOG: An International Journal of Obstetrics & Gynaecology, 95: 323–326. doi: 10.1111/j.1471-0528.1988.tb06599.x
Publication History
- Issue published online: 19 AUG 2005
- Article first published online: 19 AUG 2005
- Received 5 January 1987 Accepted I8 June 1987
- Abstract
- References
- Cited By
Summary. Eighty-three patients with twin pregnancies were seen at the University Hospital of Rotterdam between 1 January 1980 and 31 August 1985 for prenatal genetic studies. No abnormal karyotypes were found. Amniotic fluid was successfully obtained from both amniotic sacs in 77 patients. In two pregnancies elevated levels of alpha-fetoprotein (AEP) were found in both sacs. One of these pregnancies was terminated and the other continued until term. One pregnancy miscarried 4 weeks after amniocentesis at 19 weeks gestation; three women were delivered between 23 and 28 weeks, 36 at between 28 and 37 weeks and 42 women after 37 weeks. The perinatal mortality rate was 55/1000 (9 of 164). These results show that genetic amniocentesis is a safe and reliable technique in twin pregnancy but the interpretation of elevated AFP levels is complicated by the fact that AFP diffuses across the amniotic membranes between the two sacs.

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