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一名成人发生内脏异位和左心室心肌致密化不全的罕见病例。

A rare case of heterotaxy and left ventricular non-compaction in an adult.

作者信息

Chacko A, Scholtz L, Vedajallam S, van Wyk C

机构信息

Department of Radiology, Steve Biko Academic Hospital, University of Pretoria, Pretoria, South Africa.

Scholtz & Partners, Diagnostic Radiologists, Pretoria, South Africa.

出版信息

Cardiovasc J Afr. 2016 Jan-Feb;27(1):45-8. doi: 10.5830/CVJA-2015-063. Epub 2015 Aug 31.

Abstract

Heterotaxy syndrome with left ventricular non-compaction is a rare co-existence of abnormalities with unknown cause. It can be isolated with no other associations, or associated with congenital heart diseases, or it can occur with multiple other congenital abnormalities. We describe the third reported case of heterotaxy syndrome with left ventricular non-compaction presenting in an adult.

摘要

合并左心室心肌致密化不全的内脏异位综合征是一种病因不明的罕见的异常共存情况。它可以单独存在而无其他关联,或与先天性心脏病相关,或者可伴有多种其他先天性异常。我们报告了第三例成人患者出现的合并左心室心肌致密化不全的内脏异位综合征。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/147b/4817066/709793d3219f/cvja-27-46-g001.jpg

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