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
Laboratory testingAlpha(1)-antitrypsin deficiency is characterized by a pathologic reduction of the serum concentration of alpha(1)-antitrypsin, the most important antiprotease in . It is one of the most common in Caucasians. Approximately 2% of are caused by alpha(1)-antitrypsin deficiency. ...
网络抗胰蛋白酶缺乏 网络释义 1. 抗胰蛋白酶缺乏 α1-抗胰蛋白酶缺乏(alpha-l-antitrypsin deficiency)是一种伴有慢性肝脏病变的常染色体隐性遗传疾病,在儿童代谢性疾病中最为 … www.transplantation.org.cn|基于 1 个网页
产品别名: Alpha-1-Antichymotrypsin; AACT-Alpha 1; AACT Alpha 1; SERPINA3; AACT; A1ACT; ACT; Alpha 1 Antichymotrypsin 1; Alpha 1 Antichymotrypsin 2; Alpha 1 Antichymotrypsin 3; Alpha 1 Antitrypsin Deficiency; Anti Elastase; Antichymotrypsin; Cell growth inhibiting gene 24/25 protein; Clade A ...
Diagnosis of alpha-1 antitrypsin deficiency often begins with a chest X-ray or Chest CTto look for hyperinflated(过度膨胀)lungs or evidence of damaged lung tissue. 一般诊断的话肺就看胸片或者CT,或者找到一些肺损伤的证据 In addition, pulmonary function testing can be used to measure how quickly ...
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 来自 国家科技图书文献中心 喜欢 0 阅读量: 15 作者:Hatipoglu,Umur,Stoller,James,K.摘要: alpha(1)-Antitrypsin deficiency is an autosomal co 关键词: alpha(1)-AntitryPsin deficiency Emphysema Cirrhosis Diagnostic testing Targeted detection Augmentation therapy ...
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...
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(1)-Antitrypsin deficiency (AATD) is an autosomal-codominant genetic disorder that predisposes individuals to the development of liver and lung disease. AATD is greatly underrecognized and underdiagnosed. Early identification allows preventive measures to be taken, the most important of which is th...