Discordant results between fetal karyotyping and non‐invasive prenatal testing by maternal plasma sequencing in a case of uniparental disomy 21 due to trisomic …

M Pan, FT Li, Y Li, FM Jiang, DZ Li, TK Lau… - Prenatal …, 2013 - Wiley Online Library
M Pan, FT Li, Y Li, FM Jiang, DZ Li, TK Lau, C Liao
Prenatal diagnosis, 2013Wiley Online Library
Uniparental disomy (UPD) is an uncommon chromosome condition, but UPD involving
chromosome 21 is rarely reported. We reported here a case who had first trimester
screening test for Down syndrome, chorionic villus sampling for fetal karyotyping,
quantitative fluorescence polymerase chain reaction (QF‐PCR), as well as non‐invasive
prenatal testing (NIPT) by maternal plasma sequencing. There were discordant results
between fetal karyotyping and NIPT due to UPD 21combined with confined placental …
Abstract
Uniparental disomy (UPD) is an uncommon chromosome condition, but UPD involving chromosome 21 is rarely reported. We reported here a case who had first trimester screening test for Down syndrome, chorionic villus sampling for fetal karyotyping, quantitative fluorescence polymerase chain reaction (QF‐PCR), as well as non‐invasive prenatal testing (NIPT) by maternal plasma sequencing. There were discordant results between fetal karyotyping and NIPT due to UPD 21combined with confined placental mosaicism of trisomy 21. This demonstrated that it is possible to detect placental mosaicism by NIPT, but further studies are required to confirm its sensitivity. Therefore, all positive NIPT results must be confirmed by conventional invasive test and karyotyping. QF‐PCR has the additional benefit in diagnosing UPD. © 2013 John Wiley & Sons, Ltd.
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