Abstract
A 15 year old boy with sickle cell disease developed intrahepatic cholestasis. A course of exchange transfusion successfully corrected the extreme hyperbilirubinaemia over one year. Upon stopping the exchange transfusion programme the hyperbilirubinaemia relapsed but transfusion was effective when reinstituted.
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APA
O’Callaghan, A., O’Brien, S. G., Ninkovic, M., Butcher, G. P., Foster, C. S., Walters, J. R. F., & Roberts, I. A. G. (1995). Chronic intrahepatic cholestasis in sickle cell disease requiring exchange transfusion. Gut, 37(1), 144–147. https://doi.org/10.1136/gut.37.1.144
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