Alpha-1抗胰蛋白酶缺乏症的英文名字是Alpha-1 antitrypsin deficiency。基因解码表明:Alpha-1抗胰蛋白酶缺乏症是一种遗传性疾病,与基因突变密切相关。 Alpha-1抗胰蛋白酶是一种由SERPINA1基因编码的蛋白质,它在肝脏中合成并通过血液循环分布到全身。该蛋白质的主要功能是抑制胰蛋白酶的活性,以保护肺部组织免受胰蛋白...
Alpha-1 Antitrypsin Deficiency Family Study Α1-抗胰蛋白酶缺乏症慢性阻塞性肺疾病慢性阻塞性肺病遗传性疾病家系世界卫生组织COPD摘要:生命科学:英文版OsorioRaquelFemandesHelenaCafofoTomasiaClementeHelenaFialhoLicinio
Alpha-1 antitrypsin(抗胰蛋白酶)deficiency is a genetic disorder(遗传病)in which a protein called alpha-1antitrypsin is defective or absent, and it causes lung and liver disease. α抗胰蛋白酶缺乏症是一种遗传性疾病,患者体内的一种叫做α抗胰蛋白酶的蛋白质出现了问题或者含量减少了,最终导致肺和肝脏...
alpha-1-antitrypsin deficiency lessons from longevity 青云英语翻译 请在下面的文本框内输入文字,然后点击开始翻译按钮进行翻译,如果您看不到结果,请重新翻译! 翻译结果1翻译结果2翻译结果3翻译结果4翻译结果5 翻译结果1复制译文编辑译文朗读译文返回顶部 α- 1抗胰蛋白酶缺乏症的教训,从长寿...
Feelings of isolation can be common among people diagnosed with a rare disease. But Dee Kroecker, who is living with the rare genetic condition Alpha 1 Antitrypsin Deficiency, wants newly diagnosed patients to know that they are not alone. ...
ALPHA 1 ANTITRYPSIN DEFICIENCY IN THE PATHOGENESIS (OF BRONCHOPULMONARY DYSPLASIABronchopulmonary Dysplasia (BPD) is a major cause of neonatal respiratory morbidity and mortality. The pathophysiology of BPD may be related to an absence of the antiprotease alpha 1 anti-trypsin (αLat) in pulmonary ...
Alpha-1 Antitrypsin Deficiency (A1AD) is a hereditary condition characterized by low levels of circulating alpha-antitrypsin (AAT) in plasma. It is the best understood genetic risk factor for the development of chronic obstructive pulmonary disease (COPD). The diagnosis of A1AD is under-recognized...
alpha-1antitrypsindeficiency网络甲一型抗胰蛋白酶缺乏症;甲一型抗胰蛋白缺乏症;甲一型抗胰蛋白酵素缺乏症 网络释义 1. 甲一型抗胰蛋白酶缺乏症 ... · 甲一型抗胰蛋白酶缺乏症( Alpha-1 antitrypsin deficiency , AAT deficiency) · 囊胞性纤维症( Cystic fibrosis , CF) ... baike.soso.com|基于45...
Of 200,000 Swedish infants screened for alpha 1-antitrypsin deficiency (alpha 1 ATD), 184 (127 PiZ, 2 PiZ-, 54 PiSZ, and 1 PiS-) children have been followed prospectively, of whom 1 PiSZ and 5 PiZ children died in early childhood. We now... T Sveger,S Eriksson - 《Hepatology》 ...
Seven persons with homozygous deficiency of alpha1 antitrypsin and 23 related family members were studied. It was possible to differentiate homozygous deficient, heterozygous, and normal persons by determination of total trypsin inhibitory capacity of the serum and immunodiffusion of serum in variable dil...