Prenatal Diagnosis of Placental Mesenchymal Dysplasia with 46, X, Isochromosome Xq/45, X Mosaicism

Chin Chieh Hsu, Chien Hong Lee, Shuenn Dyh Chang, Tsang Ming Ko, Shir Hwa Ueng, Yu Hsiu Chen, Mei Chia Wang, Yao Lung Chang*

*Corresponding author for this work

Research output: Contribution to journalJournal Article peer-review

Abstract

Placental mesenchymal dysplasia is an uncommon vascular anomaly of the placenta with characteristics of placentomegaly and multicystic appearance and with or without association with fetal chromosomal anomaly. We present a unique placental mesenchymal dysplasia patient with amniotic fluid karyotyping as 46, X, iso(X) (q10). Detailed molecular testing of the amniotic fluid, fetal cord blood, non-dysplastic placenta and dysplastic placenta was conducted after termination of pregnancy, from which we proved biparental/androgenetic (46, X, i(X) (q10)/45, X) mosaicism in different gestational tissues. A high portion of androgenetic cells in dysplastic placenta (74.2%) and near 100% of biparental cells in the fetus’s blood and amniotic fluid were revealed. Delicate mosaic analyses were performed, and possible pathogenesis and embryogenesis of this case were drawn up.

Original languageEnglish
Article number245
JournalGenes
Volume13
Issue number2
DOIs
StatePublished - 02 2022

Bibliographical note

Publisher Copyright:
© 2022 by the authors. Licensee MDPI, Basel, Switzerland.

Keywords

  • 45 X
  • Array CGH
  • Biparental/androgenetic mosaicism
  • Isochromosome X
  • Karyotype
  • Microsatellite
  • Placental mesenchymal dysplasia
  • Short tandem repeats

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