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美洲印第安人乳糖酶缺乏症的家族研究。

Family studies of lactase deficiency in the American Indian.

作者信息

Newcomer A D, Gordon H, Thomas P J, McGill D B

出版信息

Gastroenterology. 1977 Nov;73(5):985-8.

PMID:908510
Abstract

To determine the pattern of inheritance of lactase deficiency, we studied 104 American Indian and 2 white subjects in 19 families. Subjects were considered deficient in lactase if breath-hydrogen excretion exceeded 0.20 ml per min above fasting at 2 hr after a lactose load of 2 g per kg of body weight (maximum 50 g). Seventy-one per cent of the males and 75% of the females were lactase deficient. In three families in which both parents were lactase normal, 40% of the children were lactase deficient; and in the three families with one parent lactase normal and the other lactase deficient, 65% of the children were deficient in lactase; and finally, in the seven families with both parents lactase deficient, 93% of the children were lactase deficient. This distribution of lactase deficiency in the families suggests that this trait shows an autosomal-recessive pattern of inheritance.

摘要

为了确定乳糖酶缺乏症的遗传模式,我们对19个家庭中的104名美国印第安人和2名白人受试者进行了研究。如果在每公斤体重给予2克乳糖负荷(最大50克)后2小时,呼气中氢气排泄量超过空腹时每分钟0.20毫升,则受试者被认为乳糖酶缺乏。71%的男性和75%的女性乳糖酶缺乏。在父母双方乳糖酶均正常的三个家庭中,40%的孩子乳糖酶缺乏;在父母一方乳糖酶正常而另一方乳糖酶缺乏的三个家庭中,65%的孩子乳糖酶缺乏;最后,在父母双方乳糖酶均缺乏的七个家庭中,93%的孩子乳糖酶缺乏。家庭中乳糖酶缺乏症的这种分布表明,该性状呈现常染色体隐性遗传模式。

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