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伴有罕见心脏异常的波特综合征。

Potter syndrome with an unusual cardiac anomaly.

作者信息

Prabhu Savit, Sigamani Elanthenral, Das Prasenjit, Sasi Arun, Safaya Rajni

机构信息

Department of Pathology, All India Institute of Medical Sciences, New Delhi 110029, India.

出版信息

BMJ Case Rep. 2009;2009:bcr0120091518. doi: 10.1136/bcr.01.2009.1518. Epub 2009 Apr 1.

Abstract

Potter syndrome is a congenital anomaly characterised by bilateral renal agenesis, pulmonary hypoplasia, cardiac, skeletal abnormalities and maternal oligohydramnios. Here we report a case of Potter syndrome with bilateral renal agenesis, pulmonary hypoplasia and complete transposition of the great vessels, which had been identified during a post-mortem examination. Although cardiac anomalies are known to exist with Potter syndrome, complete transposition of the great vessels has not been reported in the literature.

摘要

波特综合征是一种先天性异常,其特征为双侧肾缺如、肺发育不全、心脏和骨骼异常以及母体羊水过少。在此,我们报告一例波特综合征病例,该病例伴有双侧肾缺如、肺发育不全和大动脉完全转位,这是在尸检过程中发现的。虽然已知波特综合征存在心脏异常,但大动脉完全转位在文献中尚未见报道。

相似文献

1
Potter syndrome with an unusual cardiac anomaly.伴有罕见心脏异常的波特综合征。
BMJ Case Rep. 2009;2009:bcr0120091518. doi: 10.1136/bcr.01.2009.1518. Epub 2009 Apr 1.
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Rare manifestations of Potter Sequence: A Case Report.罕见的 Potter 序列表现:病例报告。
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本文引用的文献

1
Facial characteristics of infants with bilateral renal agenesis.双侧肾缺如婴儿的面部特征。
Am J Obstet Gynecol. 1946 Jun;51:885-8. doi: 10.1016/s0002-9378(16)39968-9.
2
Transposition of the great arteries.大动脉转位
Orphanet J Rare Dis. 2008 Oct 13;3:27. doi: 10.1186/1750-1172-3-27.

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