Norwood W I, Lang P, Casteneda A R, Campbell D N
J Thorac Cardiovasc Surg. 1981 Oct;82(4):511-9.
Aortic atresia is a form of congenital cardiac disease complicated by associated severe hypoplasia of the ascending aorta and various degrees of mitral valve and left ventricular hypoplasia. Occasionally, neonates with severe aortic stenosis have associated severe hypoplasia of the ascending aorta and left ventricle. These two defects constitute the most prevalent forms of so-called hypoplastic left heart syndrome. At present, this lesion is universally fatal with no established surgical management. This report describes our experience with the evolution and evaluation of staged surgical management of infants with hypoplastic left heart syndrome.
主动脉闭锁是一种先天性心脏病，常伴有升主动脉严重发育不全以及不同程度的二尖瓣和左心室发育不全。偶尔，患有严重主动脉狭窄的新生儿也会伴有升主动脉和左心室严重发育不全。这两种缺陷构成了所谓左心发育不全综合征最常见的形式。目前，这种病变如不进行手术治疗普遍会导致死亡。本报告描述了我们对左心发育不全综合征婴儿进行分期手术治疗的进展及评估经验。
