Neonatal Hematology 2005
DOI: 10.1017/cbo9780511545306.008
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Hemolytic disease of the fetus and newborn

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Cited by 5 publications
(4 citation statements)
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“…Third group was of other blood group HDN categorized as non-RhD and non ABO HDN, where other blood group irregular antibodies in the mother's serum were detected by indirect coomb's test (ICT) and corresponding antigen present on neonate RBCs were detected by DCT & ICT using polyspecific Coomb's serum. Other than RhD and ABO antibodies, the most common and significant antibodies causing HDN are RhC, Rhc, RhE, Kell I (K) Kell II (k), Js b , Fy a M, S & V [17,22]. Antibodies usually associated with mild to moderate HDN are Kp a , Kp b , LW, JK a , JK b , JK3, Js a , Ula, (Kel 10) Fy3, etc.…”
Section: Discussionmentioning
confidence: 99%
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“…Third group was of other blood group HDN categorized as non-RhD and non ABO HDN, where other blood group irregular antibodies in the mother's serum were detected by indirect coomb's test (ICT) and corresponding antigen present on neonate RBCs were detected by DCT & ICT using polyspecific Coomb's serum. Other than RhD and ABO antibodies, the most common and significant antibodies causing HDN are RhC, Rhc, RhE, Kell I (K) Kell II (k), Js b , Fy a M, S & V [17,22]. Antibodies usually associated with mild to moderate HDN are Kp a , Kp b , LW, JK a , JK b , JK3, Js a , Ula, (Kel 10) Fy3, etc.…”
Section: Discussionmentioning
confidence: 99%
“…Antibodies usually associated with mild to moderate HDN are Kp a , Kp b , LW, JK a , JK b , JK3, Js a , Ula, (Kel 10) Fy3, etc. [17,22]. Vengelem Tyler V [23] studied and discussed 64 different RBC antibodies specificities reported to cause HDN.…”
Section: Discussionmentioning
confidence: 99%
“…The American Academy of Pediatrics recommended use of IVIG for hemolytic disease of the fetus and newborn which was associated with a decreased need for exchange transfusion for term and preterm infants with Rh and ABO incompatibility [2]. IVIG is used at a dose up to 1-2 g/kg.…”
Section: Discussionmentioning
confidence: 99%
“…Maternal antibodies can continue to mediate HDFN following birth. While most antibodies do not remain detectable beyond 8–12 weeks post‐partum, moderate to severe cases can be characterized by hemolysis lasting beyond this timeframe 3,4 . Rare cases of persistent HDFN have been suggested to be secondary to passive transfer of maternal antibodies via breast milk 5–9 .…”
Section: Introductionmentioning
confidence: 99%