Association of aberrant right subclavian artery with abnormal karyotype and microarray results

Prenat Diagn. 2017 Aug;37(8):808-811. doi: 10.1002/pd.5092. Epub 2017 Jul 12.

Abstract

Objectives: The objective of this study is to evaluate the incidence of chromosomal aberration (both microscopic and sub-microscopic) in fetuses with an aberrant right subclavian artery (ARSA) detected by ultrasonographic anomaly scan.

Methods: The study included 62 pregnant women whose fetuses were diagnosed with ARSA who were referred for genetic counseling. Of these, 55 patients underwent amniocentesis and 7 declined invasive testing. All 55 amniocentesis samples were tested by standard G-banding and chromosomal microarray, except for 2 samples for which only karyotype and fluorescence in situ hybridization for 22q11.2 deletions were performed.

Results: Of the 55 women who underwent amniocentesis, 5 were detected with trisomy 21 (9.1%), all of whom had additional ultrasound findings. Among the 14 fetuses with ARSA and additional ultrasound findings, the incidence of trisomy 21 was 35.7%. In fetuses with isolated ARSA, no chromosomal aberrations were detected by standard cytogenetic analysis and only one (1.9%) deleterious copy number variants (CNV) was detected by chromosomal microarray.

Conclusion: Aberrant right subclavian artery with additional ultrasound findings constitute a strong predictor for aneuploidy. However, when ARSA is found in isolation, it confers no increased risk for aneuploidy or pathogenic CNVs. © 2017 John Wiley & Sons, Ltd.

MeSH terms

  • Aneurysm / diagnostic imaging
  • Aneurysm / genetics*
  • Cardiovascular Abnormalities / diagnostic imaging
  • Cardiovascular Abnormalities / genetics*
  • DiGeorge Syndrome / diagnostic imaging*
  • Female
  • Humans
  • Pregnancy
  • Subclavian Artery / abnormalities*
  • Subclavian Artery / diagnostic imaging
  • Ultrasonography, Prenatal

Supplementary concepts

  • Aberrant subclavian artery