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A rare case of hemolytic disease of newborn due to weak D (D unknown) antigen in child

机译:儿童D(D未知)抗原弱导致罕见的新生儿溶血病

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We are reporting a rare case of hemolytic disease of newborn with weak D antigen in child. A 3rd order male child of G3P3A0 mother was admitted at 8th h of life with jaundice. Blood group of both mother and child were A Rh D negative. Baby's direct coombs test was positive. Weak D antigen was positive in baby. Hematological parameters showed all the signs of ongoing hemolysis, and the bilirubin level was in the zone of exchange transfusion. Exchange transfusion was done. An intravenous immunoglobulin was given to child after that. Mother had a history of first normal healthy male child with O Rh D positive blood group. Second male child expired on 3rd postnatal day due to bilirubin encephalopathy that had A Rh D negative blood group with positive direct coombs test.
机译:我们报道了少儿D抗原弱的新生儿溶血病病例。 G 3 P 3 A 0 母亲的3 rd 顺序男婴于第8 入院黄疸的生活。母子血型均为A Rh D阴性。婴儿的直接库仑试验呈阳性。婴儿中弱D抗原呈阳性。血液学参数显示正在进行溶血的所有迹象,并且胆红素水平处于交换输血区。交换输血完成。然后给孩子静脉注射免疫球蛋白。母亲有第一个正常健康的男性儿童,其O Rh D阳性血型。由于胆红素脑病的A Rh D阴性血型,直接库仑试验阳性,第二名男婴在出生后第3天死亡。

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