Monozygotic twins discordant for trisomy 21 and maternal 21q inheritance: A complex series of events

Authors


  • How to cite this article: Dahoun S, Gagos S, Gagnebin M, Gehrig C, Burgi C, Simon F, Vieux C, Extermann P, Lyle R, Morris MA, Antonarakis SE, Béna F, Blouin J-L. 2008. Monozygotic twins discordant for trisomy 21 and maternal 21q inheritance: A complex series of events. Am J Med Genet Part A 146A:2086–2093.

  • Sophie Dahoun and Sarantis Gagos contributed equally to the work.

Abstract

We report on a monochorionic/diamniotic twin pregnancy discordant for trisomy 21. Amniocentesis (at equation image weeks) was performed following ultrasound signs of hydrops and cystic hygroma in twin 1 (T1). Prenatal karyotype showed non-mosaic trisomy 21 in T1 (47,XX,+21[7]), and low-grade mosaic trisomy 21 in twin 2 (T2) (47,XX,+21[2]/46,XX[19]). Post mortem examination of fetal skin, kidneys and lungs confirmed trisomy 21 in T1 (47,XX,+21[548]) and the placenta (47,XX,+21[200]). T2 had a normal karyotype (46,XX[648]). Analysis of microsatellite polymorphisms in multiple samples from the placenta, hand, lungs, kidneys and the umbilical cords of both twins confirmed monozygosity for all loci tested, and trisomy 21 in T1. Unexpectedly, T1 and T2 inherited different maternal alleles for markers of the most distal 4 Mbp of 21q. At least four successive events are needed to explain the genetic status of both twins and include maternal MI premature chromatids separation or maternal II meiotic nondisjunction and post-zygotic events such as, chromosome rescue, nondisjunction, an/or recombination. © 2008 Wiley-Liss, Inc.

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