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Non-Invasive Prenatal Screening: The First Report of Pentasomy X Detected by Plasma Cell-Free DNA and Karyotype Analysis.

Luigia De FalcoTeresa SueroGiovanni SavaresePasquale SavareseRaffaella RuggieroAntonella Di CarloMariasole BrunoNadia PetrilloMonica IannielloCiro ScarpatoCamilla SarliAntonio Fico
Published in: Diagnostics (Basel, Switzerland) (2022)
Pentasomy X is a sex chromosome anomaly caused by the presence of three extra X chromosomes in females (49,XXXXX instead of 46,XX) and is probably due to a nondisjunction during the meiosis. So far, only five cases prenatally diagnosed were described. The main features in 49,XXXXX karyotype include severe intellectual disability with delayed speech development, short stature, facial dysmorphisms, osseous and articular abnormalities, congenital heart malformations, and skeletal and limb abnormalities. Prenatal diagnosis is often difficult due to the lack of a clear echographic sign like nuchal translucency (NT), and mostly cases were postnatally described. We report the first case of a 49,XXXXX female that was detected by non-invasive prenatal screening (NIPS), quantitative fluorescence polymerase chain reaction (QF-PCR) and a fetal karyotype.
Keyphrases
  • intellectual disability
  • autism spectrum disorder
  • pregnant women
  • high resolution
  • early onset
  • copy number
  • gene expression
  • energy transfer
  • soft tissue
  • genome wide
  • quantum dots