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Two cases of confined placental mosaicism for chromosome 4, including one with maternal uniparental disomy.

机译:2例4号染色体的局限性胎盘镶嵌术,其中1例为母亲单亲二体性。

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摘要

Two cases of trisomy 4 mosaicism are reported including one with molecularly confirmed uniparental disomy (UPD) of chromosome 4. Cytogenetic analysis of a chorionic villus sample (CVS) in Case 1 showed complete trisomy 4 in trophoblast and diploidy in chorionic stroma. Amniotic fluid analysis demonstrated a 46,XX complement. After intrauterine fetal death at 30 weeks, molecular analysis confirmed the presence of trisomy 4 of maternal meiotic origin, while fetal tissues showed maternal UPD for chromosome 4. Cultured CVS in Case 2 revealed trisomy 4 in 2/30 cells analyzed. This pregnancy resulted in a healthy livebirth with biparental inheritance of chromosome 4. Molecularly confirmed UPD4 has not been previously reported, and therefore, although the adverse outcome in Case 1 is likely due to the trisomy 4 in the placenta, an imprinting effect associated with UPD4 cannot be excluded. Copyright 2001 John Wiley & Sons, Ltd.
机译:据报道有2例三体性4号嵌合体,其中1例具有分子确证的4号染色体单亲二体性(UPD)。细胞遗传学分析表明,病例1的绒毛膜绒毛样本(CVS)完整,在滋养层中有4号三体性,在绒毛膜基质中有二倍体。羊水分析显示补体为46,XX。子宫内胎儿在30周内死亡后,分子分析证实存在母本减数分裂起源的三体性4号染色体,而胎儿组织显示4号染色体的母体UPD。案例2中培养的CVS显示在所分析的2/30细胞中存在三体性4号。该妊娠导致健康的分娩,双亲遗传了4号染色体。先前尚未报道过分子确诊的UPD4,因此,尽管病例1的不良结局很可能是由于胎盘中的三体性4,与UPD4相关的印迹效应不能排除。版权所有2001 John Wiley&Sons,Ltd.

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