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Haemoglobin SD disease--rare case of jaundice

Ghosh, U.C.; Sen, K.; Narayan, A.; Banik, K.K.; Saha, P.K.

Journal of the Indian Medical Association 110(7): 501-502

2012

ISSN/ISBN: 0019-5847
PMID: 23520682
Document Number: 661038
A 15 years old Muslim female presented with moderate anaemia, mild jaundice and hepatosplenomegaly with no history of blood transfusion in the past. Routine examination was suggestive of haemolytic jaundice. High pressure liquid chromatography (HPLC) electrophoresis of the patient's blood showed haemoglobin (Hb) SD disease. As it is a double heterozygous disease, family screening was done. It showed that the father was sickle cell trait. Mother was Hb D trait. Both the brothers were sickle cell trait and the only sister was normal. Hb SD disease is a very rare variety of haemoglobinopathy and the case is presented here due to its rarity.

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