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

Abstract

About 15% to 20% of all clinically recognized pregnancies result in spontaneous abortion or miscarriage, and chromosomal anomalies can be identiἀed in up to 50% of ἀrst trimester miscarriages. Chromosomal microarray analysis (CMA) is currently considered ἀrst-tier testing for detecting fetal chromosomal abnormalities and is supported by the absence of cell culture fail-ure 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 ἀrst trimester spontaneous abortions. Here, we report two cases of triploidy abortion that were not detected using array compara-tive 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.