4.0 Editorial Material

Apical hypertrophic cardiomyopathy with subendocardial late gadolinium enhancement in an adolescent

期刊

CARDIOLOGY IN THE YOUNG
卷 31, 期 2, 页码 286-288

出版社

CAMBRIDGE UNIV PRESS
DOI: 10.1017/S1047951120004692

关键词

Pediatric cardiomyopathy; cardiovascular magnetic resonance; genetics

向作者/读者索取更多资源

A 17-year-old boy with a history of dyspnea attacks and chest pain was diagnosed with apical hypertrophic cardiomyopathy, revealed through cardiovascular magnetic resonance imaging. The rare diagnosis was missed by echocardiography, highlighting the importance of different imaging modalities in diagnosing cardiac conditions.
A 17-year-old boy with a history of dyspnea attacks and chest pain was referred to our paediatric cardiology department. Electrocardiogram at presentation showed T-wave inversion in the inferior leads. Cardiovascular magnetic resonance imaging revealed the rare diagnosis of apical hypertrophic cardiomyopathy with subendocardial late gadolinium enhancement, missed by echocardiography.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.0
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据