Congenital Haemolytic Anaemia with early onset and uncommon presentation: A Case Report
DOI:
https://doi.org/10.3329/cbmj.v6i2.54729Keywords:
Haemoglobin disorder, congenital haemolytic anaemia, PBF, Hb electrophoresisAbstract
Haemolytic anaemias result from an increase in the rate of red cell destruction. The lifespan of the normal red cell is 100-120 days; in the haemolytic anaemias it is shortened by varying degrees, and in very severe cases may be only a few days. Here we described a male child of 1.5 months presented with yellow coloration of whole body and sclera since birth, progressive pallor since birth & gradual abdominal distention for 20 days. The child was admitted to hospital with the complaints of bleeding from mouth and nose for 3 days. Peripheral blood film of the child showed features of hemolytic anaemia, as a congenital hemolytic anaemia probably hemoglobinopathies/thalassemia. As because the child is 1.5 months old the diagnosis was confirmed by Hb-electrophoresis of his parents. Hb-electrophoresis examination of the parent showed predominant Hb was HbE which was 90.0% found in mother & 92.4% found in father. So the case was diagnosed as congenital hemolytic anaemia, HbE disease.
CBMJ 2017 July: Vol. 06 No. 02 P: 32-37
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