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自动分析仪测定慢性肉芽肿病(CGD)患者及杂合子携带者的红细胞凯尔血型表型。

Auto analyzer determination of red cell Kell phenotypes in patients with chronic granulomatous disease (CGD) and heterozygous carriers.

作者信息

Bowell P J, Hill F G

出版信息

Br J Haematol. 1978 Jul;39(3):351-5. doi: 10.1111/j.1365-2141.1978.tb01107.x.

Abstract

One of six boys chronic granulomatous disease was shown to have the rare Kell phenotype, McLeod, by both manual and Auto Analyzer techniques. Using the Auto Analyzer, the red cells of this boy's mother were clearly shown to have weaker expression of k and Kpb antigens than those of the controls, whereas the Kell groups on the father's red cells appeared normal.

摘要

通过手工和自动分析仪技术,在六名患有慢性肉芽肿病的男孩中,有一名被发现具有罕见的凯尔血型,即麦克劳德血型。使用自动分析仪时,该男孩母亲的红细胞显示出k和Kpb抗原的表达明显弱于对照组,而其父亲红细胞上的凯尔血型分组看起来正常。

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2
Chronic granulomatous disease and the Kell blood groups.慢性肉芽肿病与凯尔血型系统
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Hereditary acanthocytosis associated with the McLeod phenotype of the Kell blood group system.
Br J Haematol. 1979 Aug;42(4):575-83. doi: 10.1111/j.1365-2141.1979.tb01170.x.

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