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Molecular genotyping of hydatidiform moles: analytic validation of a multiplex short tandem repeat assay.葡萄胎的分子基因分型:多重短串联重复序列分析的验证。
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2
Complete hydatidiform mole with retained maternal chromosomes 6 and 11.完全性葡萄胎伴母源6号和11号染色体保留。
Am J Surg Pathol. 2009 Sep;33(9):1409-15. doi: 10.1097/PAS.0b013e3181a90e01.
3
Diagnosis and subclassification of hydatidiform moles using p57 immunohistochemistry and molecular genotyping: validation and prospective analysis in routine and consultation practice settings with development of an algorithmic approach.使用p57免疫组织化学和分子基因分型对葡萄胎进行诊断和亚分类:在常规和会诊实践环境中的验证及前瞻性分析,并开发算法方法
Am J Surg Pathol. 2009 Jun;33(6):805-17. doi: 10.1097/PAS.0b013e318191f309.
4
Meiotic errors in human oogenesis and spermatogenesis.人类卵子发生和精子发生过程中的减数分裂错误。
Reprod Biomed Online. 2008 Apr;16(4):523-31. doi: 10.1016/s1472-6483(10)60459-2.
5
Diagnostic problems with trophoblastic lesions.滋养层病变的诊断问题。
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The origin of human aneuploidy: where we have been, where we are going.人类非整倍体的起源:我们来自何处,又将去往何方。
Hum Mol Genet. 2007 Oct 15;16 Spec No. 2:R203-8. doi: 10.1093/hmg/ddm243.
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Clinical characteristics of persistent gestational trophoblastic neoplasia after partial hydatidiform molar pregnancy.部分性葡萄胎妊娠后持续性滋养细胞肿瘤的临床特征
J Reprod Med. 2006 Nov;51(11):902-6.
8
Persistent gestational trophoblastic neoplasia after partial hydatidiform mole incidence and outcome.部分性葡萄胎后持续性妊娠滋养细胞肿瘤的发生率及结局
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9
A father of four consecutive trisomic pregnancies with elevated frequencies of associated aneuploid sperm.一位有四次连续三体妊娠且伴有非整倍体精子频率升高的父亲。
Am J Med Genet A. 2006 Sep 1;140A(17):1840-5. doi: 10.1002/ajmg.a.31391.
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Meiotic chromosome abnormalities in human spermatogenesis.人类精子发生过程中的减数分裂染色体异常。
Reprod Toxicol. 2006 Aug;22(2):142-7. doi: 10.1016/j.reprotox.2006.03.013. Epub 2006 May 22.

与父源性三三体相关的异常绒毛形态。

Abnormal villous morphology associated with triple trisomy of paternal origin.

机构信息

Department of Pathology, The Johns Hopkins Medical Institutions, Baltimore, Maryland, USA.

出版信息

J Mol Diagn. 2010 Jul;12(4):525-9. doi: 10.2353/jmoldx.2010.090184. Epub 2010 Apr 22.

DOI:10.2353/jmoldx.2010.090184
PMID:20413680
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2893639/
Abstract

The vast majority of trisomies in spontaneous abortions (SAB) are single and of maternal origin, most frequently due to meiosis I errors. Triple trisomies are exceedingly rare (approximately 0.05% of spontaneous abortions), most often of maternal origin, and associated with increased maternal age. Some trisomic SAB specimens can exhibit abnormal villous morphology simulating a partial hydatidiform mole, a distinct form of hydatidiform mole characterized by diandric triploidy. A SAB specimen from a 27-year-old woman, G1P0 at 8 weeks gestational age, was reviewed in consultation to address the finding of morphological features suggestive of a partial hydatidiform mole but DNA ploidy analysis yielding a diploid result. The villi were irregularly shaped and hydropic but lacked trophoblastic hyperplasia; p57 expression was retained. Since fully developed features of a partial hydatidiform mole were lacking, additional analysis was performed. Molecular genotyping and single nucleotide polymorphism array analysis demonstrated biparental diploidy with trisomy of chromosomes 7, 13, and 20, all of paternal origin. The three trisomies may have originated from paternal meiosis II errors, or from mitotic nondisjunction. We believe this to be the first report of triple trisomy in a SAB confirmed to be of paternal origin.

摘要

自发性流产(SAB)中的绝大多数三体都是单倍体,且来源于母体,最常见的原因是减数分裂 I 错误。三倍体极为罕见(约占自发性流产的 0.05%),通常来源于母体,并与母亲年龄增加有关。一些三体 SAB 标本可表现出异常的绒毛形态,类似于部分葡萄胎,这是一种独特的葡萄胎形式,其特征为二倍体三倍体。一名 27 岁的初产妇,孕 8 周,G1P0,行 SAB 检查,形态学上提示部分葡萄胎,但 DNA 倍性分析结果为二倍体,因此会诊以明确诊断。绒毛形状不规则,呈囊泡状水肿,但无滋养层细胞增生;p57 表达保留。由于部分葡萄胎的完全特征不明显,因此进行了进一步的分析。分子基因分型和单核苷酸多态性微阵列分析显示,存在双亲二倍体和 7、13 和 20 号染色体三体,均来源于父系。这三个三体可能源自父源减数分裂 II 错误,或源自有丝分裂不分离。我们认为这是首例父源性三倍体 SAB 的报道。