Failure to Predict Hemolysis and Hyperbilirubinemia by IgG Subclass in Blood Group A or B Infants Born to Group O Mothers
Author:
Affiliation:
1. Department of Neonatology
2. Faculty of Medicine, Hebrew University, Jerusalem, Israel
3. Blood Bank, Shaare Zedek Medical Center, Jerusalem, Israel
4. Department of Pediatrics, Stanford University School of Medicine, Stanford, California
Abstract
Publisher
American Academy of Pediatrics (AAP)
Subject
Pediatrics, Perinatology and Child Health
Link
https://publications.aap.org/pediatrics/article-pdf/123/1/e132/1124285/zpe0010900e132.pdf
Reference23 articles.
1. Grundbacher FJ. The etiology of ABO hemolytic disease of the newborn. Transfusion. 1980;20(5):563–568
2. American Academy of Pediatrics Subcommittee on Hyperbilirubinemia. Management of hyperbilirubinemia in the newborn infant 35 or more weeks of gestation [published correction appears in Pediatrics. 2004;114(4):1138]. Pediatrics. 2004;114(1):297–316
3. Ozolek JA, Watchko JF, Mimouni F. Prevalence and lack of clinical significance of blood group incompatibility in mothers with blood type A or B. J Pediatr. 1994;125(1):87–91
4. Meberg A, Johansen KB. Screening for neonatal hyperbilirubinaemia and ABO alloimmunization at the time of testing for phenylketonuria and congenital hypothyreosis. Acta Paediatr. 1998;87(12):1269–1274
5. Ukita M, Takahashi A, Nunotani T, Kihana T, Watanabe S, Yamada N. IgG subclasses of anti-A and anti-B antibodies bound to the cord red cells in ABO incompatible pregnancies. Vox Sang. 1989;56(3):181–186
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