A Case Report of Rapid Progressive Coarctation and Severe Middle Aortic Syndrome in an Infant with Williams Syndrome

被引：9

作者：

Hall, E. Kevin ^{[1
]}

Glatz, Jenifer ^{[1
]}

Kaplan, Paige ^{[2
]}

Kaplan, Bernard S. ^{[3
]}

Hellinger, Jeffrey ^{[4
]}

Ernst, Linda ^{[5
]}

Gaynor, J. William ^{[6
]}

机构：

[1] Childrens Hosp Philadelphia, Div Cardiol, Philadelphia, PA 19104 USA

[2] Childrens Hosp Philadelphia, Div Metab Dis, Philadelphia, PA 19104 USA

[3] Childrens Hosp Philadelphia, Div Nephrol, Philadelphia, PA 19104 USA

[4] Childrens Hosp Philadelphia, Div Radiol, Philadelphia, PA 19104 USA

[5] Childrens Hosp Philadelphia, Div Pathol & Lab Med, Philadelphia, PA 19104 USA

[6] Childrens Hosp Philadelphia, Div Cardiothorac Surg, Philadelphia, PA 19104 USA

来源：

CONGENITAL HEART DISEASE | 2009年 / 4卷 / 05期

关键词：

Coarctation; Middle Aortic Syndrome; Williams Syndrome; STENOSIS; PATIENT; ELASTIN;

D O I：

10.1111/j.1747-0803.2009.00287.x

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

Williams syndrome is a genetic disorder caused by multiple contiguous gene deletions in chromosome 7. Presentation in early life is most often a result of luminal stenosis of right- and left-sided arterial vasculature. We report the case of a newborn infant who had a rapidly progressing diffuse form of arteriopathy that required two surgeries and one percutaneous balloon dilation within the first 2 months of her life.

引用

页码：373 / 377

页数：5

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