A fatal case of idiopathic restrictive cardiomyopathy
A fatal case of idiopathic restrictive cardiomyopathy
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DOI：
10.1017/s1047951103000970
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发表时间：
2003-10-01
影响因子：
1
通讯作者：
Ward, C
中科院分区：
文献类型：
--
作者：
Palka, P;Lange, A;Ward, C
我们描述了一个女婴的特发性限制性心肌病的临床特征。左心室舒张末期压显著升高，心肌舒张功能异常，与多普勒血流超声心动图，再加上多普勒组织超声心动图相对较新的技术检测。没有持续心力衰竭的临床证据，但她有心肌缺血的迹象，不幸在13个月大时突然死亡。
We describe the clinical features of idiopathic restrictive cardiomyopathy in a female infant. A marked elevation of left ventricular end-diastolic pressure, and profoundly abnormal myocardial relaxation, were detected with the use of Doppler blood flow echocardiography, coupled with the relatively new technique of Doppler tissue echocardiography. There was no clinical evidence of ongoing heart failure, but she had signs of myocardial ischaemia, and unfortunately died suddenly at the age of 13 months.