Does Gγ/Aγ ratio and Hb F level influence the severity of sickle cell anaemia

Sickle cell anaemia (SCA) exhibits significant variations in clinical presentation in different populations for which several genetic factors including SCA-associated alpha- and beta-thalassaemias, G-6-PD deficiency and elevated Hb F level have been implicated as possible ameliorating factors. Saudi...

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Veröffentlicht in:Molecular and cellular biochemistry 1993-07, Vol.124 (1), p.17-22
Hauptverfasser: EL-HAZMI, M. A. F, BAHAKIM, H. M, WARSY, A. S, ABDULKARIM AL-MOMEN, ABDULLAH AL-WAZZAN, IBRAHIM AL-FAWWAZ, SAMEER HURAIB, MOHAMMAD HARAKATI
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Sprache:eng
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Zusammenfassung:Sickle cell anaemia (SCA) exhibits significant variations in clinical presentation in different populations for which several genetic factors including SCA-associated alpha- and beta-thalassaemias, G-6-PD deficiency and elevated Hb F level have been implicated as possible ameliorating factors. Saudi Arabia is unique in that mild and severe forms of the disease occur at a high frequency. We investigated the G gamma/A gamma ratio and Hb F level and correlated these values with the severity of SCA. The results showed that Hb F level varies significantly in both groups of patients with no evident correlation with the mild clinical manifestations. However, G gamma/A gamma ratio correlated significantly with the disease severity where a high ratio was observed in patients with the mild and a low ratio in patients with the severe disease. The results are evaluated and discussed in the light of correlation studies and regression analysis.
ISSN:0300-8177
1573-4919
DOI:10.1007/BF01096377