| Literature DB >> 4642791 |
A van Enk, A Lang, J M White, H Lehmann.
Abstract
Two Ghanaian women with sickle-cell anaemia and alpha-thalassaemia were found to have an unusually benign obstetric history. In addition to two factors present which are known to moderate the clinical course of sickle-cell anaemia, good socioeconomic status and a relatively high Hb F level, it is suggested that alpha-thalassaemia may act among other things by lowering the haemoglobin concentration in the red cells and thereby lowering their tendency to sickle in vivo.Entities:
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Year: 1972 PMID: 4642791 PMCID: PMC1788764 DOI: 10.1136/bmj.4.5839.524
Source DB: PubMed Journal: Br Med J ISSN: 0007-1447