J Genet Med.  2019 Dec;16(2):76-80. 10.5734/JGM.2019.16.2.76.

Triploidy that escaped diagnosis using chromosomal microarray testing in early pregnancy loss: Two cases and a literature review

• Park JE
• Park JK
• Kang MY
• Jo HC
• Cho IA
• Baek JC

• KMID: 2470102
• DOI: http://doi.org/10.5734/JGM.2019.16.2.76

Abstract

About 15% to 20% of all clinically recognized pregnancies result in spontaneous abortion or miscarriage, and chromosomal anomalies can be identified in up to 50% of first trimester miscarriages. Chromosomal microarray analysis (CMA) is currently considered first-tier testing for detecting fetal chromosomal abnormalities and is supported by the absence of cell culture failure or erroneous results due to cell contamination in pregnancy loss. Triploidy is a lethal chromosome number abnormality characterized by an extra haploid set of chromosomes. Triploidy is one of the most common chromosomal aberrations in first trimester spontaneous abortions. Here, we report two cases of triploidy abortion that were not detected using array comparative genomic hybridization-based CMA. The aim of this report was to remind clinicians of the limitations of chromosomal testing and the misdiagnosis that can result from biased test selection.

Keyword

Comparative genomic hybridization; Microarray analysis; Karyotyping; Abortion; spontaneous; Triploidy

MeSH Terms

Abortion, Spontaneous
Bias (Epidemiology)
Cell Culture Techniques
Chromosome Aberrations
Comparative Genomic Hybridization
Diagnosis*
Diagnostic Errors
Female
Haploidy
Humans
Karyotyping
Microarray Analysis
Pregnancy Trimester, First
Pregnancy*
Triploidy*
United Nations*