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直接胆红素血症并发新生儿ABO溶血病。

Direct hyperbilirubinemia complicating ABO hemolytic disease of the newborn.

作者信息

Sivan Y, Merlob P, Nutman J, Reisner S H

出版信息

Clin Pediatr (Phila). 1983 Aug;22(8):537-8. doi: 10.1177/000992288302200802.

DOI:10.1177/000992288302200802
PMID:6683136
Abstract

A retrospective study of the diagnostic implications of conjugated hyperbilirubinemia complicating ABO hemolytic disease of the newborn (HDN) was done by studying the records of 264 infants with ABO-HDN. Direct hyperbilirubinemia was found to complicate ABO-HDN in 3 per cent of the infants, all being full term. Eighty-seven per cent were female and familial occurrence was noted in half of the cases. Most of the infants presented with anemia on the first day of life. Our data suggest that this is a benign complication of ABO-HDN which clears within a month.

摘要

通过研究264例ABO血型新生儿溶血病(HDN)患儿的病历,对新生儿ABO血型溶血病合并结合胆红素血症的诊断意义进行了一项回顾性研究。发现3%的患儿ABO-HDN合并直接胆红素血症,均为足月儿。其中87%为女性,半数病例有家族发病情况。大多数患儿在出生第一天就出现贫血。我们的数据表明,这是ABO-HDN的一种良性并发症,一个月内可消退。

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1
Direct hyperbilirubinemia complicating ABO hemolytic disease of the newborn.直接胆红素血症并发新生儿ABO溶血病。
Clin Pediatr (Phila). 1983 Aug;22(8):537-8. doi: 10.1177/000992288302200802.
2
ABO hemolytic disease of the newborn associated with direct reacting hyperbilirubinemia.与直接反应性高胆红素血症相关的新生儿ABO溶血病。
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Study of Gilbert's Syndrome-Associated UGT1A1 Polymorphism in Jaundiced Neonates of ABO Incompatibility Hemolysis Disease.ABO 血型不合溶血病高胆红素血症新生儿 Gilbert 综合征相关 UGT1A1 多态性研究。
Am J Perinatol. 2020 May;37(6):652-658. doi: 10.1055/s-0039-1688816. Epub 2019 May 14.
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ABO hemolytic disease of the newborn. A retrospective analysis of 254 cases.新生儿ABO溶血病。254例回顾性分析。
Am J Clin Pathol. 1980 Mar;73(3):369-73. doi: 10.1093/ajcp/73.3.369.
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Early diagnosis of ABO haemolytic disease of the newborn.新生儿ABO溶血病的早期诊断
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[FamiliaL hemolytic disease in the newborn infant with direct hyperbilirubinemia].新生儿直接胆红素血症伴家族性溶血性疾病
Ann Pediatr (Paris). 1986 Apr;33(4):359-61.
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[Practical and clinical problems in hemolytic disease of the newborn].新生儿溶血病的实际与临床问题
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Familial occurrence of hemolytic disease of the newborn due to AO blood group incompatibility.由于AO血型不相容导致的新生儿溶血病的家族性发病情况。
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Risk factors for readmission for hyperbilirubinemia in neonates with ABO hemolytic disease: a single-center retrospective cohort study.ABO溶血病新生儿高胆红素血症再入院的危险因素:一项单中心回顾性队列研究。
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Conjugated hyperbilirubinemia in infants with erythroblastosis fetalis.
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Rapid Identification of Biallelic Mutation in a Neonate with Severe Congenital Hemolytic Anemia and Liver Failure.
一名患有严重先天性溶血性贫血和肝功能衰竭的新生儿双等位基因突变的快速鉴定
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Cholestasis in a neonate with ABO haemolytic disease of newborn following transfusion of ABO group-specific red cells compatible with neonatal serum: inspissated bile syndrome.在一名患有新生儿ABO溶血病的新生儿输注与新生儿血清相容的ABO血型特异性红细胞后发生胆汁淤积:浓缩胆汁综合征。
Blood Transfus. 2014 Oct;12(4):621-3. doi: 10.2450/2014.0099-14.