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血红蛋白M海德公园作为一种新突变出现:诊断、结构和遗传学考量

Haemoglobin M Hyde Park occurring as a fresh mutation: diagnostic, structural, and genetic considerations.

作者信息

Stamatoyannopoulos G, Nute P E, Giblett E, Detter J, Chard R

出版信息

J Med Genet. 1976 Apr;13(2):142-7. doi: 10.1136/jmg.13.2.142.

Abstract

Hb M Hyde Park disease was detected in a girl who for several years was thought to have cyanotic heart disease. The problems of recognizing the condition are outlined and clues to diagnosis are discussed. Evidence for heme loss from the aberrant beta chains of Hb M Hyde Park and production of an unstable molecule is presented. The normal haematological findings in the patient's parents, as well as their blood groups and isozymes, suggest that the occurrence of her Hb M Hyde Park was the result of a fresh mutation.

摘要

在一名多年来被认为患有青紫型心脏病的女孩身上检测到了血红蛋白M海德公园病。文中概述了识别该病症的问题,并讨论了诊断线索。文中还提供了证据,证明血红蛋白M海德公园异常β链存在血红素丢失以及产生了不稳定分子。患者父母正常的血液学检查结果,以及他们的血型和同工酶,表明她患血红蛋白M海德公园病是新突变的结果。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/be7b/1013374/fcd03dd315b2/jmedgene00309-0064-a.jpg

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