Han K S, Kim H C, Han K S, Shim W S
Department of Clinical Pathology, Seoul National University College of Medicine, Korea.
Am J Perinatol. 1997 Sep;14(8):495-7. doi: 10.1055/s-2007-994188.
-D- is a rare haplotype that determines D without C, c, E or e, and exalted D activity. The extremely rare homozygote propositi (-D-/-D-) are usually ascertained through their immune antibodies, anti-Rh17 (Hro), which react with red cells of all common Rh phenotypes. The authors experienced the first case in Korea of a woman with -D- phenotype. She had a history of spontaneous abortion, therapeutic termination and red cell transfusion, and at her third pregnancy she delivered a baby with severe hemolytic disease of the newborn. In spite of intensive medical intervention, the baby died of hydrops fetalis. An immune antibody to high incidence Rh antigen, namely anti-Rh17(Hro), was demonstrated in the woman's serum. A family study revealed that the -D- gene complex was present in all its members and one of the woman's sisters was also -D- homozygote. In the serum of this sister, anti-Rh17(Hro) was also present.
-D-是一种罕见的单倍型,它决定了D抗原的存在,而没有C、c、E或e抗原,并且具有增强的D活性。极其罕见的纯合子先证者(-D-/-D-)通常是通过其免疫抗体抗-Rh17(Hro)被确定的,该抗体可与所有常见Rh表型的红细胞发生反应。作者遇到了韩国首例-D-表型女性病例。她有自然流产、治疗性终止妊娠和红细胞输血史,在第三次怀孕时,她生下了一名患有严重新生儿溶血病的婴儿。尽管进行了积极的医疗干预,婴儿仍死于胎儿水肿。在该女性血清中检测到了针对高发生率Rh抗原的免疫抗体,即抗-Rh17(Hro)。家族研究表明,-D-基因复合体存在于其所有成员中,该女性的一个姐妹也是-D-纯合子。在这个姐妹的血清中也存在抗-Rh17(Hro)。