在两个明显健康的孕妇中偶然发现的全基因组纯合子镶嵌现象。

IF 1.7 4区 生物学 Q3 GENETICS & HEREDITY
Gloria T Haskell, S Hussain Askree, Laura Kline, Linda Hasadsri, Huong Cabral, Inder Gadi, Stuart Schwartz
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引用次数: 0

摘要

当一条染色体或染色体片段的两个拷贝仅来自一个亲本时,就会发生单倍体(UPD)。马赛克全基因组UPD(大多数gwUPD)通常在胎儿死亡和胎盘发育不良或产前病例中发现,其中印记效应与异常超声结果相关。由于upd相关的印迹效应(特别是Beckwith-Wiedemann综合征),已经报道了大多数gwUPD和临床特征的儿童;然而,关于成人重度gwUPD的报道很少。在这里,我们描述了两个明显健康的成年孕妇的大部分gwUPD。携带者测试发现,在正常杂合范围之外,变异的等位基因比例偏斜,这促使进一步的测试。单核苷酸多态性(SNP)微阵列鉴定了gwUPD在两个个体中的嵌合体,分别在血液中存在85%和90%,在其他组织中存在不同的百分比。两名女性在检测时均未表现出gwUPD应有的临床特征,尽管回顾性仔细的个人病史是一致的。这两名妇女都顺利怀孕,并生下了足月健康的婴儿。这两个病例表明,大多数gwUPD可能是在表面健康的成年女性中偶然发现的。临床随访对于肿瘤监测、遗传咨询和未来妊娠监测非常重要,因为大多数gwUPD存在于母体子宫内膜组织中。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Mosaicism for Genome Wide Homozygosity Identified as an Incidental Finding in Two Apparently Healthy Pregnant Women.

Uniparental Disomy (UPD) occurs when both copies of a chromosome or chromosomal segment originate from only one parent. Mosaic genome-wide UPD (mos gwUPD) is typically identified in cases of fetal demise and placental dysplasia or in prenatal cases, where imprinting effects are associated with abnormal ultrasound findings. Children with mos gwUPD and clinical features due to UPD-associated imprinting effects (especially Beckwith-Wiedemann syndrome) have been reported; however, reports of adults with mos gwUPD are rare. Here we describe mos gwUPD in two apparently healthy pregnant adult women. Carrier testing noted variants with skewed allelic ratios outside of the normal heterozygous range, prompting further testing. Single nucleotide polymorphism (SNP) microarray identified mosaicism for gwUPD in both individuals, present at 85% and 90%, respectively, in blood, with varying percentages in other tissues. Neither woman displayed clinical features that would be expected with gwUPD at the time of testing, although retrospective careful personal history was consistent. Both women had uneventful pregnancies and delivered full-term healthy infants. These two cases demonstrate that mos gwUPD can be an incidental finding identified in apparently healthy adult women. Clinical follow-up is important for tumor monitoring, genetic counseling, and monitoring of future pregnancies due to mos gwUPD in the maternal endometrial tissue.

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来源期刊
CiteScore
3.50
自引率
5.00%
发文量
432
审稿时长
2-4 weeks
期刊介绍: The American Journal of Medical Genetics - Part A (AJMG) gives you continuous coverage of all biological and medical aspects of genetic disorders and birth defects, as well as in-depth documentation of phenotype analysis within the current context of genotype/phenotype correlations. In addition to Part A , AJMG also publishes two other parts: Part B: Neuropsychiatric Genetics , covering experimental and clinical investigations of the genetic mechanisms underlying neurologic and psychiatric disorders. Part C: Seminars in Medical Genetics , guest-edited collections of thematic reviews of topical interest to the readership of AJMG .
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