Results of 180 First Trimester Direct Chromosome Studies in Chorionic Villi

  • E. S. Sachs
  • J. O. Van Hemel
  • M. G. J. Jahoda
  • H. Galjaard

Abstract

First trimester fetal chromosome analysis has been successfully carried out for 180 patients in our center. Cytogenetic studies of chorionic villi have been greatly facilitated by the observation of Brambati and Simoni (1983) that direct preparations after sampling are possible. This method is a great improvement for parents at high risk of producing offspring with anomalies, such as carriers of a translocation or an X-linked disease. Termination of pregnancy in the case of an abnormal fetal karyotype is now possible at 9 weeks instead of at 19 weeks of gestation, after the cultivation of amniotic fluid cells. We report here the results of 180 pregnancies at risk for a chromosomal anomaly or an X-linked disease, with special emphasis on unbalanced fetal translocations, the demonstration of a fragile X chromosome in villi and DNA linkage studies of a male fetus at risk for Duchenne’s muscular dystrophy.

Keywords

Chorionic Villus Male Fetus Chorionic Villus Sampling Amniotic Fluid Cell Translocation Carrier 
These keywords were added by machine and not by the authors. This process is experimental and the keywords may be updated as the learning algorithm improves.

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Copyright information

© Springer-Verlag Berlin Heidelberg 1985

Authors and Affiliations

  • E. S. Sachs
    • 1
  • J. O. Van Hemel
    • 1
  • M. G. J. Jahoda
    • 2
  • H. Galjaard
    • 1
  1. 1.Dept. of Clinical GeneticsErasmus Universiteit RotterdamDR RotterdamThe Netherlands
  2. 2.Academic Hospital Rotterdam DijkzigtRotterdamThe Netherlands

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