肺动脉闭锁的遗传学基础与临床
摘要
肺动脉闭锁(pulmonary atresia,PA)为一种较少见的紫绀型先天性心脏病(先心病),发病率占先天性心脏病的1.0%~1.5%;肺动脉闭锁可仅限于肺动脉瓣,亦可为肺动脉干、1支或2支中央肺动脉。
出处
《中华胸心血管外科杂志》
CSCD
北大核心
2012年第2期108-109,共2页
Chinese Journal of Thoracic and Cardiovascular Surgery
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