查询词典 deficiency

There are also many pediatric liver disease, including biliary atresia, alpha-1 antitrypsin deficiency, alagille syndrome, and progressive familial intrahepatic cholestasis, to name but a few.

还有许多儿童肝脏疾病，包括胆道闭锁、阿尔法-1抗缺失，郁积综合症家族性肝内胆汁和进步，是名副其实的。

The statement came in response to claims by Ian Halperin, an unauthorised biographer, that Jackson is suffering from a rare genetic condition called Alpha-1 antitrypsin deficiency.

这篇声明是为了回应Ian Halperin，一位非法自传作者，所声称的&杰克逊得了少见的遗传疾病，叫做Alpha-1抗胰蛋白酶缺乏症&。

Known as Alpha-1 antitrypsin deficiency (A1AD), a potentially fatal genetic illness.

大明星病情严重的流言的始作俑者是作家Ian Halperin。

Genetic analysis shows that antitrypsin deficiency appeared only about 2000 years ago in Northern Germany and was transferred from Scandinavia by the Vikings."The gene has been retained, I think, because it causes inflammation, because in the old days people died because of gastroenteritis," Dr. Lomas told attendees."So my idea is that this mutation was protective — until people started smoking."

基因分析显示抗胰蛋白酵素缺损在约2000年前首见於北德，系由北欧海盗从斯堪的那维亚半岛传播而来；Lomas博士告诉听众，我认为基因被保留，因为它引起发炎、人们在古老年代会死於肠胃炎，所以我的想法是，此一突变是有保护效果的—直到人们开始抽菸为止。

Alpha-1 antitrypsin deficiency, hemochromatosis, Wilson's disease, galactosemia, and glycogen storage diseases are among the inherited diseases that interfere with the way the liver produces, processes, and stores enzymes, proteins, metals, and other substances the body needs to function properly.

阿尔法-1抗缺失，血色素、威尔森氏症、半乳糖、糖原贮藏疾病、遗传性疾病等方面的干扰肝脏产生方式、程序、商店、酵素、蛋白质、金属和其他物质的身体需要好好地运作。

Cirrhosis may also be caused by metabolic diseases (Wilson's disease, hemochromatosis, and alpha 1 - antitrypsin deficiency, all of which can be diagnosed by laboratory tests and/or liver biopsy) or toxins (diagnosed by positive history for drugs, environmental or industrial toxins, and confirmatory lab investigation).

硬化也可由代谢疾病引起（威尔逊氏病，血色沉着病，α-1型胰岛素缺乏症，以上均可在实验室检验或经肝活检确诊）或由毒素引起（可以经用药史，接触环境或工业毒素史，或实验室检查判断）。

Alpha-1 antitrypsin is the most abundant circulating protease inhibitor in the body, Dr. Lomas said. Its most common deficiency mutation is the Z allele, where the amino acid lysine is exchanged for glutamic acid at position 342 in the polypeptide chain (Glu342Lys). About 1 in 1700 whites of northern European descent are homozygotes for this mutation and thus have plasma antitrypsin levels that are 10% to 15% below normal, he said.

Lomas博士表示，甲一型抗胰蛋白酵素是身体内最充分的循环蛋白酶抑制剂，最常见的缺损突变在Z对偶基因，该处的胺基酸 lysine与麸氨酸在多胜肽链的第342位置交换(Glu342Lys)；北欧血统白人每1，700人有1人是此一突变的同合子，因此血浆抗胰蛋白酵素值比正常低10%到15%。

Investigative journalist Ian Halperin recently told In Touch weekly that Michael Jackson has a very severe lung condition called "Alpha-1 antitrypsin deficiency", and needs a lung transplant but may be too weak to go through with it.

调查记者哈普林最近向《In Touch》周刊透露，迈克尔·杰克逊患上了一种罕见的肺病，叫做&甲一型抗胰蛋白酵素缺乏症&，由于病况严重，迈克尔需要肺部移植，但他身体太弱，手术风险很高。

Objective: To study the rate of the combined tests of thalassemia and G6PD deficiency in detection of before marriage, to direct aristogenesis and good brood.

目的探讨地中海贫血和G6PD缺乏联合检测在婚前检查中的发病率，并指导优生优育。

Objective: To study the rate of the combined tests of thalassemia and G6PD deficiency in detection of before marriage, to direct aristogenesis and good brood.

文章摘要：目的探讨地中海贫血和G6PD缺乏联合检测在婚前检查中的发病率，并指导优生优育。

Neither the killing of Mr Zarqawi nor any breakthrough on the political front will stop the insurgency and the fratricidal murders in their tracks.

在对危险的南部地区访问时，他斥责什叶派民兵领导人对中央集权的挑衅行为。

In fact,I've got him on the satellite mobile right now.

实际上 我们已接通卫星可视电话了