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儿童期早期的α1-抗胰蛋白酶缺乏症(作者译)

[alpha 1-Antitrypsin deficiency in early childhood (author's transl)].

作者信息

Osswald P, Gathmann H

出版信息

Leber Magen Darm. 1979 Sep;9(5):241-6.

PMID:93226
Abstract

alpha 1-Antitrypsin inhibits various proteases and excessive proteolysis. If serum and tissue concentrations of this compound are low throughout longer periods of time due to deficient synthesis, - which is a dominantly inherited trait, - progressive pulmonary emphysema will develop in adults, and liver disease in more than 50% of the cases in infancy and early childhood. Three subtypes can be distinguished: the heaptitis type, the intrahepatic hypoplasia of the bile duct system, and the cholangitic type which may imitate atresia of bile ducts. Prognosis of the liver disease depends upon the time, at which inflammatory processes stop, excessive proteolysis coming to a stop at the same time. No treatment is known for this disease.

摘要

α1-抗胰蛋白酶可抑制多种蛋白酶和过度的蛋白水解。如果由于合成不足,该化合物的血清和组织浓度在较长时间内一直较低(这是一种显性遗传特征),成年人会发展为进行性肺气肿,婴儿期和幼儿期超过50%的病例会出现肝病。可区分出三种亚型:肝炎型、胆管系统肝内发育不全型和可能类似胆管闭锁的胆管炎型。肝病的预后取决于炎症过程停止的时间,此时过度的蛋白水解也会同时停止。目前尚无针对该疾病的治疗方法。

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