1600-0609/asset/EJH_left.gif?v=1&s=9cc42688299494a2f6f3f67d6d96cfe04346d96b)
Decreased red cell enolase activity in a 40-year-old woman with compensated haemolysis
Article first published online: 24 APR 2009
DOI: 10.1111/j.1600-0609.1984.tb00716.x
© Munksgaard 1984
1600-0609/asset/cover.gif?v=1&s=946b5b431efb8410b6fa87b6a03da604c501f5f7 "Scandinavian Journal of Haematology")
Additional Information
How to Cite
Boulard-Heitzmann, P., Boulard, M., Tallineau, C., Boivin, P., Tanzer, J., Bois, M. and Barriere, M. (1984), Decreased red cell enolase activity in a 40-year-old woman with compensated haemolysis. Scandinavian Journal of Haematology, 33: 401–404. doi: 10.1111/j.1600-0609.1984.tb00716.x
Publication History
- Issue published online: 24 APR 2009
- Article first published online: 24 APR 2009
- Accepted for publication May 2, 1984
- Abstract
- References
- Cited By
Keywords:
- enolase;
- enzyme defect;
- haemolysis;
- red cell
A 40-year-old woman splenectomized 17 years previously for hereditary haemolytic anaemia was investigated in our laboratory because of persistent conjunctival subic-terus associated with compensated haemolysis. The results of the autohaemolysis and osmotic fragility tests were similar to those usually observed in hereditary spherocytosis. Red cell enzyme assays indicated a decreased amount of kinetically normal enolase. The genetic transmission of this defect could not be established since the only other affected member of the family was the proposita's father who died several years ago after splenectomy for an undefined haemolytic disorder.