Babiker MA, El Seed FA
A family with sickle cell trait and hereditary spherocytosis. [Journal Article]
Scand J Haematol 1984 Jul; 33(1):54-8.
The rare combination of sickle cell trait with hereditary spherocytosis in a Sudanese family is reported. The splenic hypofunction and fibrosis as a result of sickling has ameliorated the clinical course of the 35 year old father. The symptoms of a six years old son seem to be getting milder with age too. The family is managed conservatively and splenectomy was not required.
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