Wolff-Parkinson-White (WPW) syndrome in isolated noncompaction of the ventricular myocardium (INVM) - Three cases

被引：28

作者：

Nihei, K ^{[1
]}

Shinomiya, N ^{[1
]}

Kabayama, H ^{[1
]}

Ikeda, C ^{[1
]}

Hosono, T ^{[1
]}

Aoki, T ^{[1
]}

Matsuo, N ^{[1
]}

机构：

[1] Toho Univ, Sch Med, Dept Pediat 2, Tokyo, Japan

来源：

CIRCULATION JOURNAL | 2004年 / 68卷 / 01期

关键词：

cardiomyopathy; isolated noncompaction of the ventricular myocardium; right anteroseptal pathway; Wolff-Parkinson-White syndrome type B;

D O I：

10.1253/circj.68.82

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

Isolated noncompaction of the ventricular myocardium (INVM) is a rare morphological abnormality caused by cessation of the compaction of the loose interwoven meshwork of myocardial fibers during intrauterine life. Three cases of INVM, including 2 siblings, were diagnosed from 2-dimensional echocardiographic findings of Wolff-Parkinson-White syndrome type B to which INVM can be attributed.

引用

页码：82 / 84

页数：3

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