Article
Hereditary ovalocytosis with compensated haemolysis.
British journal of haematology - 1 Sept 1993
Reardon D M, Seymour C A, Cox T M, Pinder J C, Schofield A E, Tanner M J
Abstract excerpt
The clinical and laboratory phenotype of compensated haemolysis in a patient with hereditary ovalocytosis is reported. Clinical presentation was intermittent jaundice and abdominal pain due to pigment gall stones. Haematological analysis revealed an absolute reticulocytosis with an otherwise normal full blood count and biochemical evidence of haemolysis. Variable results were observed with blood grouping...
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