دورية
aThalassemia and the Hematology of Homozygous Sickle Cell Disease in Childhood
| العنوان: | aThalassemia and the Hematology of Homozygous Sickle Cell Disease in Childhood |
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| المؤلفون: | Stevens, M.C.G., Maude, G.H., Beckford, M., Grandison, Y., Mason, K., Taylor, B., Serjeant, B.E., Higgs, D.R., Teal, H., Weatherall, D.J., Serjeant, G.R. |
| المصدر: | Blood; February 1986, Vol. 67 Issue: 2 p411-414, 4p |
| مستخلص: | aThalassemia modifies the hematologic expression of homozygous sickle cell (SS) disease, resulting in increased total hemoglobin and HbA2and decreased HbF, mean cell volume, reticulocytes, irreversibly sickled cells, and bilirubin levels. The age at which these changes develop in children with SS disease is unknown. Ascertainment of globin gene status in a large representative sample of children with SS disease has afforded an opportunity to study the hematologic indices in nine children homozygous for athalassemia 2 (two-gene group), 90 children heterozygous for athalassemia 2 (three-gene group), and 167 children with a normal aglobin gene complement (four-gene group). The two-gene group had significantly lower mean cell volumes from birth, higher red cell counts from one month, lower reticulocytes from three months, and higher HbA2 levels from one year, as compared with the four-gene group. Children with three genes had intermediate indices but resembled more closely the four-gene group. Differences in total hemoglobin or in fetal hemoglobin between the groups were not apparent by eight years of age. The most characteristic differences of the two-gene group were the raised proportional HbA2 level and low mean cell volume, the latter having some predictive value for a thalassemia status at birth. © 1986 by Grune & Stratton, Inc. |
| قاعدة البيانات: | Supplemental Index |
| تدمد: | 00064971 15280020 |
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| DOI: | 10.1182/blood.V67.2.411.411 |