Abstract
The blood picture of children with sickle-cell anaemia was found to change with age. The changes were most marked in the first year but the mean level of haemoglobin, haemoglobin F, and target cells fell until adolescence, and irreversibly sickled cells rose. Reticulocytes, Howell Jolly bodies, and normablasts altered little after one year. The fall in haemoglobin F suggested a delayed changeover from fetal to adult haemoglobin production. It was concluded that the blood changes in sickle-cell anaemia were progressive throughout childhood.
Full text
PDF



Selected References
These references are in PubMed. This may not be the complete list of references from this article.
- Davis L. R. Target cells in haemoglobinopathies. J Clin Pathol. 1972 Feb;25(2):169–170. doi: 10.1136/jcp.25.2.169. [DOI] [PMC free article] [PubMed] [Google Scholar]
- JACKSON J. F., ODOM J. L., BELL W. N. Amelioration of sickle cell disease by persistent fetal hemoglobin. JAMA. 1961 Sep 23;177:867–869. doi: 10.1001/jama.1961.73040380028011b. [DOI] [PubMed] [Google Scholar]
- JENSEN W. N., RUCKNAGEL D. L., TAYLOR W. J. In vivo study of the sickle cell phenomenon. J Lab Clin Med. 1960 Dec;56:854–865. [PubMed] [Google Scholar]
- Pearson H. A., Spencer R. P., Cornelius E. A. Functional asplenia in sickle-cell anemia. N Engl J Med. 1969 Oct 23;281(17):923–926. doi: 10.1056/NEJM196910232811703. [DOI] [PubMed] [Google Scholar]
- SINGER K., CHERNOFF A. I., SINGER L. Studies on abnormal hemoglobins. I. Their demonstration in sickle cell anemia and other hematologic disorders by means of alkali denaturation. Blood. 1951 May;6(5):413–428. [PubMed] [Google Scholar]
- Serjeant G. R. Irreversibly sickled cells and splenomegaly in sickle-cell anaemia. Br J Haematol. 1970 Nov;19(5):635–641. doi: 10.1111/j.1365-2141.1970.tb01647.x. [DOI] [PubMed] [Google Scholar]