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5例9三体胎儿的产前诊断及胎儿病理检查结果

Prenatal diagnosis and fetopathological findings in five fetuses with trisomy 9.

作者信息

Chitayat D, Hodgkinson K, Luke A, Winsor E, Rose T, Kalousek D

机构信息

Prenatal Diagnosis Program, Hospital for Sick Children, Toronto, Ontario, Canada.

出版信息

Am J Med Genet. 1995 Apr 10;56(3):247-51. doi: 10.1002/ajmg.1320560302.

DOI:10.1002/ajmg.1320560302
PMID:7778583
Abstract

Five male fetuses with trisomy 9 are discussed. Three were detected prenatally and terminated, 1 aborted spontaneously, and the fifth delivered prematurely and died soon after. Multiple congenital abnormalities characteristic of trisomy 9 were detected in all 5 cases and are compared to those of previous reports.

摘要

本文讨论了5例9三体男性胎儿。其中3例在产前被检测出并终止妊娠,1例自然流产,第5例早产并在出生后不久死亡。所有5例均检测到9三体特有的多种先天性异常,并与既往报道的病例进行了比较。

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Prenatal diagnosis and fetopathological findings in five fetuses with trisomy 9.5例9三体胎儿的产前诊断及胎儿病理检查结果
Am J Med Genet. 1995 Apr 10;56(3):247-51. doi: 10.1002/ajmg.1320560302.
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引用本文的文献

1
Case report: A case report and literature review of complete trisomy 9.病例报告:9号染色体完全三体的病例报告及文献综述
Front Genet. 2023 Aug 31;14:1241245. doi: 10.3389/fgene.2023.1241245. eCollection 2023.
2
Partial trisomy 9 (9pter->9q22.1) and partial monosomy 14 (14pter- >14q11.2) due to paternal translocation t(9;14)(q22.1;q11.2) in a case of Dysmorphic features.因父亲发生t(9;14)(q22.1;q11.2)易位导致的部分9号染色体三体(9pter->9q22.1)和部分14号染色体单体(14pter->14q11.2),见于一例具有畸形特征的病例。
Intractable Rare Dis Res. 2019 Feb;8(1):72-77. doi: 10.5582/irdr.2019.01000.
3
Partial trisomy 9: prenatal diagnosis and recurrence within same family.
9号染色体部分三体:产前诊断及同一家族内复发情况
Clin Case Rep. 2017 May 10;5(6):986-992. doi: 10.1002/ccr3.970. eCollection 2017 Jun.