Counselling implications of chromosomal abnormalities other than trisomy 21 detected through a maternal serum screening programme

Br J Obstet Gynaecol. 1997 Jan;104(1):42-5. doi: 10.1111/j.1471-0528.1997.tb10647.x.

Abstract

Objective: To identify counselling requirements, we reviewed the frequency and type of non-trisomy 21 chromosome abnormalities found at amniocentesis after maternal serum screening for Down's syndrome.

Design: The study involved a review of the cytogenetic results of amniocenteses performed because of a raised maternal serum screening risk.

Setting: The maternal serum screening and amniocenteses were performed at hospitals in the Yorkshire region.

Sample: 1715 amniocenteses were performed as a result of a raised maternal serum screening risk for the period 1990 to 1993.

Methods: The cytogenetic results were classified into the main categories of numerical and structural chromosomal abnormalities.

Main outcome measures: The nature and frequency of abnormal cytogenetic results were identified in which parental samples were required in order to determine if the abnormal finding was de novo or familial and/or for which specialist genetic counselling was required.

Results: Sixty-nine pregnancies of 1715 amniocenteses were identified with a chromosomal abnormality (4.0%): 35 (2.0%) with trisomy 21 and 34 (2.0%) with another chromosomal abnormality. For 20 of these 34 abnormalities, parental karyotypes were required and in 29 of the 34 specialist genetic counselling was required.

Conclusions: Women undergoing maternal serum screening and, in particular, those proceeding to amniocentesis, should be informed that there is an equal chance that a chromosomal abnormality other than trisomy 21 will be found at amniocentesis, the nature of which usually requires parental samples and specialist counselling.

MeSH terms

  • Amniocentesis
  • Chromosome Aberrations*
  • Chromosome Inversion
  • Chromosomes, Human, Pair 13*
  • Chromosomes, Human, Pair 8*
  • Counseling*
  • Down Syndrome / diagnosis
  • Female
  • Humans
  • Karyotyping
  • Pregnancy
  • Prenatal Diagnosis*
  • Risk Factors
  • Trisomy