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双胞胎中的肝外胆道闭锁:通过短串联重复序列位点确定合子性

Extrahepatic biliary atresia in twins: zygosity determination by short tandem repeat loci.

作者信息

Poovorawan Y, Chongsrisawat V, Tanunytthawongse C, Norapaksunthorn T, Mutirangura A, Chandrakamol B

机构信息

Department of Paediatrics, Faculty of Medicine, Chulalongkorn University, Bangkok, Thailand.

出版信息

J Med Assoc Thai. 1996 Dec;79 Suppl 1:S119-24.

PMID:9071076
Abstract

Extrahepatic biliary atresia (EHBA) is an infantile obstructive cholangiopathy of unknown etiology. This condition is generally thought to be an acquired disease without familial tendency. We reported eight pairs of discordant twins in a series of 143 patients with operatively established EHBA, One pair was dizygotic twin from sex discrimination. Six were identical ABO blood groups and 2 were also the same minor blood groups (Dce, MM and Le a-b-). The last 2 sets were monzygotic twins by common DNA polymorphisms short tandem repeat loci. Our findings support the hypothesis that, EHBA is an acquired rather than a hereditary disease.

摘要

肝外胆管闭锁(EHBA)是一种病因不明的婴儿阻塞性胆管病。这种疾病通常被认为是一种无家族倾向的后天性疾病。在143例经手术确诊为EHBA的患者中,我们报告了8对不一致的双胞胎。其中一对是通过性别鉴别确定的异卵双胞胎。6对具有相同的ABO血型,2对次要血型(Dce、MM和Le a-b-)也相同。最后2对是通过常见的DNA多态性短串联重复序列位点确定的同卵双胞胎。我们的研究结果支持以下假设,即EHBA是一种后天性疾病而非遗传性疾病。

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