Coinheritance of Β-Thalassemia and Sickle Cell Anaemia in Southwestern Nigeria

dc.contributor.authorOsunkalu, VO
dc.contributor.authorBamisaye, O
dc.contributor.authorBabatunde, J
dc.contributor.authorLawal, S
dc.date.accessioned2019-12-16T14:37:03Z
dc.date.available2019-12-16T14:37:03Z
dc.date.issued2016-11
dc.description.abstractBACKGROUND: Genes for haemoglobin S are found in high frequencies in Nigeria. However, there islittle information on beta thalassemia in sickle cell anaemia in this population. The clinical presentation of HbS-β thalassemia is enormously variable, ranging from an asymptomatic state to a severe disorder similar to homozygoussickle cell disease.MATERIALS AND METHODS: Haemoglobin A2and HbF were determined in sickle cell anaemia patients attending LAUTECH Teaching Hospital, Osogbo,by elution after electrophoresis and alkaline denaturation methods respectively. Haematologicalparameters were estimated using Sysmex KX-21N and percentage target cells using Leishman’s staining technique.RESULTS: Exactly 6%f the SCA patients were found to have elevated HbA2(>3.3%) and HbF (>1.3%).These patients also had normal erythrocyte indices, increased platelet count, a significantly higher HCT and an increased % target cell.CONCLUSION: These findings confirm that the frequency of beta thalassaemia in sickle cell patients in Nigeria is higher than previously thought. It is therefore important to consider the possibility of this variant in patients with sickle cell anaemia since their course may differ from that of patients with homozygous sickle cell anaemia.en_US
dc.identifier.citationOsunkalu Vincent, Bamisaye Oluwaseyi, Babatunde James, Lawal Saidat. Coinheritance of Β-Thalassemia and Sickle Cell Anaemia in Southwestern Nigeria. Ethiop J Health Sci. 2016; Vol. 26: pg 517-22. No. 6en_US
dc.identifier.otherDOI: http://dx.doi.org/10.4314/ejhs.v26i6.3
dc.identifier.urihttps://ir.unilag.edu.ng/handle/123456789/7126
dc.language.isoenen_US
dc.publisherEthiopian Journal of Health Sciencesen_US
dc.subjectβ-Thalassemiaen_US
dc.subjectSickle cell anaemiaen_US
dc.subjectHaemoglobin A2en_US
dc.subjectHaemoglobin Fen_US
dc.titleCoinheritance of Β-Thalassemia and Sickle Cell Anaemia in Southwestern Nigeriaen_US
dc.typeArticleen_US
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