Reid J M, Houston A B, Lundmark E
Department of Cardiology, Western Infirmary, Glasgow.
Br Heart J. 1989 Nov;62(5):384-8. doi: 10.1136/hrt.62.5.384.
Hypertrophic cardiomyopathy was diagnosed in identical twin boys in early childhood. One underwent myomectomy at the age of 12 years because of progressive severe exertional dyspnoea accompanied by considerable obstruction of the left ventricular outflow tract shown on both echocardiography and cardiac catheterisation. Seven years later, at the age of 19, he remains incapacitated to a moderate degree. By contrast, the other twin has led a relatively normal life to date and no left ventricular outflow obstruction has been shown.
肥厚型心肌病在一对同卵双胞胎男孩幼儿期被诊断出来。其中一个在12岁时接受了肌瘤切除术,原因是进行性严重劳力性呼吸困难,超声心动图和心导管检查均显示左心室流出道有明显梗阻。7年后,19岁时,他仍有中度失能。相比之下,另一个双胞胎迄今为止过着相对正常的生活,未显示有左心室流出道梗阻。