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Vol. 23, No. 1, 2008   

Free Abstract     Article (References)     Article (PDF 176 KB)     

Paper

Prenatal Diagnosis of Sex Chromosome Abnormalities: The 8-Year Experience of a Single Medical Center
Zvi Vaknina, Orit Reishb, Ido Ben-Amia, Eli Heymanc, Arie Hermana, Ron Maymona

aDepartment of Obstetrics and Gynecology,
bGenetic Institute and
cDepartment of Neonatalogy, Assaf Harofeh Medical Center, Zerifin, affiliated to Sackler Faculty of Medicine, Tel-Aviv University, Tel-Aviv, Israel

Address of Corresponding Author

Fetal Diagn Ther 2008;23:76-81 (DOI: 10.1159/000109231)


 goto top of page Key Words

  • Fetal anomalies
  • Prenatal diagnosis
  • Sex chromosomal abnormalities
  • Ultrasound

 goto top of page Abstract

Objective: To assess the indications for prenatal karyotyping of sex chromosomal abnormalities (SCAs) during pregnancy. Methods: All singleton pregnancies interrupted in our institute because of SCAs (1998-2005) were categorized into subgroups of 45,XO (Turner syndrome), 47,XXY (Klinefelter syndrome), 47,XXX and 47,XYY. The indications for prenatal diagnostic testing were recorded. Results: There were 67 SCAs pregnancies: 33% Turner syndrome, 28% Klinefelter syndrome, 21% 47,XXX and 18% 47,XYY. Maternal age was similar among the 4 groups (34 ± 5, range 25-42 years). The main indications for fetal karyotyping were abnormal Down's syndrome (DS) screening or ultrasound findings, advanced maternal age (ge35 years), and parental request. About 2/3 of the Turner and 47,XYY cases had either abnormal DS screening tests or sonographic findings, such as: increased nuchal translucency, mainly cystic hygroma and fetal hydrops. However, fetal karyotyping in more than 2/3 of the 47,XXX and 47,XXY cases was mainly performed because of advanced maternal age, and the diagnosis of fetal SCAs was coincidental (p <0.03). Conclusions: Our recent suggestion to expand the DS screening capacity to other chromosomal abnormalities including SCAs is further supported. Prenatal detection seems to be promising for Turner syndrome and possibly for 47,XYY syndrome, while other SCAs are less likely to be detected either by ultrasound or biochemical screening.

Copyright © 2007 S. Karger AG, Basel


 goto top of page Author Contacts

R. Maymon, MD
Department of Obstetrics and Gynecology
Assaf Harofeh Medical Center
IL-70300 Zerifin (Israel)
Tel. +972 3 640 7443, Fax +972 3 640 9049, E-Mail intposgr@post.tau.ac.il


 goto top of page Article Information

Received: September 25, 2006
Accepted after revision: November 1, 2006
Published online: October 9, 2007
Number of Print Pages : 6
Number of Figures : 1, Number of Tables : 2, Number of References : 30

 
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Medline Abstract (ID 17934303)
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