单词biliary atresia
un.: 胆道闭锁
网络: 胆管闭锁；先天性胆道闭锁；胆道闭锁症
胆道闭锁
Biliary atresia is a birth defect in which the bile ducts do not have normal openings, preventing bile from leaving the liver.
胆道闭锁是一种不正常发育，使得胆管不能正常打开，导致胆汁不能离开肝脏产生作用。
For biliary atresia patients, this procedure offers an early operation opportunity.
对胆道闭锁患儿可以争取到早期手术的时机。
Therefore, determination of MMP-2 may reflect the prognosis of biliary atresia have the great meaning.
故测定MMP-2可能对反映胆道闭锁预后有较大意义。
Pathological changes of bile ducts and bile plugs were prominent in infants more than 3 months of age with biliary atresia.
胆道闭锁的大月龄组中胆道病变和胆栓明显，新生儿肝炎时肝细胞坏死更突出。
In addition, liver biopsies from patients with PSC and biliary atresia, had no detectable levels of FOXA2.
而且，从原发性硬化性胆管炎和胆道闭锁的患者的肝活检试样中，没有检测到FOXA2。
Seen here is the major differential diagnosis of biliary atresia: this is neonatal giant cell hepatitis.
此图为胆道闭锁的主要不同诊断：这是一例新生儿巨细胞肝炎。
We call it the obstructive jaundice, such as neonatal biliary atresia, bile viscosity and so on.
我们称它为阻塞性黄疸，如新生儿胆道闭锁、胆汁粘稠等。
Ultrastructural study on myocardial tissue in a case of congenital biliary atresia
先天性胆道闭锁患儿心肌组织的电镜观察
A comparison study of laparoscopic versus open portoenterostomy for pediatric biliary atresia
腹腔镜与开腹行肝门肠吻合术治疗小儿先天性胆道闭锁效果的对比研究
Value of duodenal secretion examination in the differential diagnosis between infantile hepatitis syndrome and biliary atresia
动态持续十二指肠液检查对婴儿肝炎综合征与先天性肝外胆道闭锁的鉴别诊断价值探讨