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BMJ Case Reports 2009; doi:10.1136/bcr.09.2008.0987
  • Rare disease

Haemolytic disease of the newborn due to anti-c

  1. Sana Abourazzak,
  2. Safae Hajjaj,
  3. Chekabab Hakima,
  4. Abdelhak Bouharrou,
  5. Moustapha Hida
  1. University Hospital Hassan II, Department of Neonatology, Service de Pédiatrie, CHU Hassan II, Fez, 30 000, Morocco
  1. abourazzak77{at}yahoo.fr
  • Published 26 February 2009

Summary

Anti-D isoimmunisation remains the most common cause of erythroblastosis fetalis. Whereas most clinically significant blood group sensitisations noted during pregnancy are still secondary to anti-D incompatibility, sensitisation to antigens other than D in the CDE system is not uncommon and can cause severe disease. The widespread use of Rh-D immune globulin has led to a relative increase in the importance of non-Rh-D isoimmunisation as a cause of haemolytic disease of the newborn. We report the case of a baby with severe hyperbilirubinaemia and persistent anaemia due to anti-c isoimmunisation with a high-titre maternal c antibody. The baby required emergency transfusion and intensive phototherapy. The medical literature relating to maternal c isoimmunisation and neonatal outcome is also reviewed. Because of its ability to cause clinically significant haemolytic disease of the newborn, practitioners must manage anti-c isoimmunisation in a manner similar to that for anti-D.

Footnotes

  • Competing interests: none.

  • Patient consent: Patient/guardian consent was obtained for publication.

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