Abstract
Reliable data for the trace element values of the biological systems in some diseases are still very rare. Sickle cell trait is one of them.
For this purpose, serum iron, zinc, and copper values, together with the total iron binding capacity and saturation percent, were determined in cases with sickle cell trait, eliminating all the sources contributing to deviations from the normal values by choosing a control group from the relatives of the cases.
In this study, the values of two groups were compared on the basis of the difference in hemoglobin type, which was the only parameter affecting the trace element analysis.
Similar content being viewed by others
References
J. Kohn,J. Clin. Pathol. 22, 109 (1969).
G. A. Daland and W. B. Castle,J. Lab. Clin. Med. 33, 1087 (1948).
W. N. M. Ramsay,Clin. Chim. Acta 2, 214 (1957).
Y. Kilinç, M. Kümi, Ö. Gezerel, L. Etiz, and F. Dönmez,North-Cyprus Symposium on Abnormal Hemoglobins and Thalassemia, 10–11 October, 1983, M. Aksoy and T. H. J. Huisman, eds., pp. 83–88.
Y. Kilinç, M. Kümi, F. Taner, and L. Etiz,North-Cyprus Symposium on Abnormal Hemoglobins and Thalassemia, 10–11 October, 1983, M. Aksoy and T. H. J. Huisman, pp. 76–82.
V. M. Buckaler, and Someren A.,Arch. Int. Med. 133, 660 (1974).
C. Natta, M. A. Weiner, H. Chang, J. A. Wolff, and R. Fawaz,J. Am. Med. Assoc. 247, 1442 (1982).
Author information
Authors and Affiliations
Rights and permissions
About this article
Cite this article
Donma, O., Yüregir, G. & Donma, M.M. Serum copper and zinc values compared with serum iron, total iron-binding capacity, and transferrin saturation in sickle cell trait. Biol Trace Elem Res 11, 37–41 (1986). https://doi.org/10.1007/BF02795522
Received:
Accepted:
Issue Date:
DOI: https://doi.org/10.1007/BF02795522