1) Cystic fibrosis
囊性纤维变性
2) cystic fibrosis (CF)
囊性纤维样变性
3) fibrocystic breast disease
乳房纤维囊性变
4) fibrosis of pancreas
胰脏囊性纤维变性
5) Cystic fibrosis
囊性纤维化
1.
The cystic fibrosis transmembrane conductance regulator(CFTR)is a chloride channel that belongs to the ATP-binding cassette(ABC)transporter superfamily.
囊性纤维化跨膜电导调节体(cystic fibrosis transmembrane conductance regulator,CFTR)是一种Cl~-通道,属ATP结合(ATP-binding cassette,ABC)转运体超家族。
2.
Mutation of CFTR which leads to cystic fibrosis will influence cell function.
囊性纤维化跨膜传导调节因子(CFTR)是一种重要的氯离子通道,突变易引起囊性纤维化病变,故得名。
3.
The etiology of CAVD is associated with the cystic fibrosis transmembrane conductance regulator(CFTR) gene and defects in the Wolffian duct, and frequently complicated by renal agenesis and other urogenital abnormalities.
研究表明 ,CAVD的发病与囊性纤维化跨膜转运调节物 (CFTR)基因突变和中肾管发育缺陷有关。
6) Fibrocystic disease
纤维囊性病
补充资料：囊性纤维变性
囊性纤维变性
cystic fibrosis
又称黏滞病或黏液黏稠病。是一种染色体隐性遗传、全身外分泌腺功能紊乱的疾病。可累及多种器官，但主要侵犯肺及消化道。临床有三大特点：弥漫性阻塞性肺病、胰腺功能不全及汗液中钠、氯浓度较正常高3～5倍。本病诊断标准为：①家族史；②典型肺部病变(慢性阻塞性肺疾患）；③胰腺功能不全；④两次汗试验阳性(汗氯＞60mmol/L）。至少有两项存在即可诊断为囊性纤维变性，但汗试验阳性为确诊所必需。
说明：补充资料仅用于学习参考，请勿用于其它任何用途。
参考词条