Partial Anomalous Left Pulmonary Artery along with Aortic Coarctation in an Infant with Kabuki Syndrome

被引：13

作者：

Bhat, Aarti H. ^{[1
]}

Davenport, Jennifer ^{[2
]}

Cocalis, Mark ^{[3
]}

机构：

[1] Univ Washington, Seattle Childrens Hosp, Div Pediat Cardiol, Seattle, WA 98105 USA

[2] Univ New Mexico, Div Pediat Cardiol, Albuquerque, NM 87131 USA

[3] Univ Calif San Francisco, Div Pediat Cardiol, UCSF Childrens Hosp, San Francisco, CA 94143 USA

来源：

ECHOCARDIOGRAPHY-A JOURNAL OF CARDIOVASCULAR ULTRASOUND AND ALLIED TECHNIQUES | 2012年 / 29卷 / 06期

关键词：

fetal coarctation; Kabuki syndrome; accessory left pulmonary artery; anomalous left pulmonary artery; pseudopulmonary artery sling; MENTAL-RETARDATION; EARS;

D O I：

10.1111/j.1540-8175.2011.01651.x

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

We report an antenatally diagnosed fetal coarctation delivered prematurely and confirmed to have coarctation as well as additional nonobstructing anomalous left pulmonary artery branch (aLPA) from right pulmonary artery (RPA) and significant dysmorphic features. The baby underwent an uncomplicated arch repair, but had numerous multisystem and growth related issues prompting a diagnosis of Kabuki syndrome (KS) at 1 year of age. While coarctation and hypoplastic left heart syndrome are observed in this syndrome, this is the second reported case of aLPA in KS and the first with the forme fruste of left-sided obstruction as well as aLPA in this group of patients. (Echocardiography 2012;29:E145-E147)

引用

页码：E145 / E147

页数：3

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