Literature DB >> 6683136

Direct hyperbilirubinemia complicating ABO hemolytic disease of the newborn.

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

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.

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Year:  1983        PMID: 6683136     DOI: 10.1177/000992288302200802

Source DB:  PubMed          Journal:  Clin Pediatr (Phila)        ISSN: 0009-9228            Impact factor:   1.168


  2 in total

1.  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.

Authors:  Ashish Jain; Ujjal Poddar; Priti Elhence; Archana Tripathi; Upendra Shava; Surender K Yachha
Journal:  Blood Transfus       Date:  2014-10       Impact factor: 3.443

2.  Rapid Identification of Biallelic SPTB Mutation in a Neonate with Severe Congenital Hemolytic Anemia and Liver Failure.

Authors:  Christopher M Richmond; Sally Campbell; Hee W Foo; Sebastian Lunke; Zornitza Stark; Amanda Moody; Elizabeth Bannister; Anthea Greenway; Natasha Brown
Journal:  Mol Syndromol       Date:  2020-02-01
  2 in total

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