先天性心脏病在婴幼儿发病率较高。常见者为室间隔缺损,法洛氏四联症及动脉导管未闭。但双腔心合并动脉导管未闭,肺动脉闭锁之先天性心脏病联合畸形实属罕见,我科收治一例,因缺乏先天性心脏病的常见杂音,致使生前未作出诊断,现报导如下。病例摘要:患儿,男性,58天,住院号205358,因生后青紫,近20天发热、咳嗽、青紫加重住院。入院时查体:体温37.6℃,呼吸72次/分,脉搏170次/分,体重3000g,全身皮 Congenital heart disease in infants and young children higher incidence. Common ventricular septal defect, tetralogy of Fallot and patent ductus arteriosus. However, double-lumen heart with patent ductus arteriosus, pulmonary atresia congenital heart disease is a rare combination of deformity, our department admitted a case, due to the lack of common murmurs of congenital heart disease, resulting in life without making a diagnosis, are reported as follows. Case Summary: Children, men, 58 days, hospital number 205358, due to bruising after birth, nearly 20 days fever, cough, bruising aggravated hospitalization. Physical examination at admission: body temperature 37.6 ℃, breathing 72 beats / min, pulse 170 beats / min, weight 3000g, whole body skin