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 norm...
Topics
- Adult
- Anion Exchange Protein 1, Erythrocyte
- Diseases in Twins
- Elliptocytosis, Hereditary
- Erythrocytes
- Hemolysis
- Humans
- Male
- Mutation
