Udskriv Udskriv
Switch language
Region Hovedstaden - en del af Københavns Universitetshospital

Trisomy 8 mosaicism in the placenta: A Danish cohort study of 37 cases and a literature review

Publikation: Bidrag til tidsskriftReviewpeer review


  1. The Phenotypic Spectrum of PRRT2-Associated Paroxysmal Neurologic Disorders in Childhood

    Publikation: Bidrag til tidsskriftTidsskriftartikelForskningpeer review

  2. Haploinsufficiency of ARHGAP42 is associated with hypertension

    Publikation: Bidrag til tidsskriftTidsskriftartikelForskningpeer review

  • Simon Horsholt Thomsen
  • Ida Charlotte Bay Lund
  • Christina Fagerberg
  • Iben Bache
  • Naja Becher
  • Ida Vogel
Vis graf over relationer

OBJECTIVE: To evaluate the risk of fetal involvement when trisomy 8 mosaicism (T8M) is detected in chorionic villus samples (CVS).

METHODS: A retrospective descriptive study of registered pregnancies in Denmark with T8M in CVS identified through a database search and a review of published cases of T8M found through a systematic literature search and inclusion of cross references. Pregnancies with T8M in CVS and no additional numerical chromosomal aberrations were included.

RESULTS: A total of 37 Danish cases and 60 published cases were included. T8M detected in a CVS was associated with fetal involvement in 18 out of 97 pregnancies (18.6% [95%CI: 11.4-27.7]). Eight out of 70 (11.4% [95%CI: 5.1-21.3]) interpreted prenatally to be confined placental mosaicism (CPM) were subsequently found to be true fetal mosaicisms (TFM).

CONCLUSION: T8M detected in CVS poses a significant risk of fetal involvement, and examination of amniotic fluid (AF) and/or fetal tissue should be offered. However, a normal result of AF still has a considerable residual risk of fetal involvement. Genetic counselling at an early gestational age is essential, and follow-up ultrasonography should be performed to predict fetal involvement if possible.

TidsskriftPrenatal Diagnosis
Udgave nummer4
Sider (fra-til)409-421
Antal sider13
StatusUdgivet - mar. 2021

Bibliografisk note

© 2020 John Wiley & Sons, Ltd.

ID: 61713497