1957
DOI: 10.1136/bmj.2.5037.143
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Relationship Between Haemoglobins C and S and Malaria in Ghana

Abstract: MMIxCALz JOURNA field and Smith, 1955), and eluted. Following starch electrophoresis the haemoglobin fractions themselves were eluted. On measuring the colour of the eluates it was found that the abnormal component formed 28% of the total haemoglobin. The proportion of haemoglobin A2 (Kunkel and Wallenius, 1955) Huisman obliged us by testing the solubility of our patient's haemoglobin by a salting-out technique; he also found it to be normal. We are grateful to Dr. Huisman for his permission to quote that t… Show more

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Cited by 22 publications
(18 citation statements)
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“…1 Early studies found that parasite prevalence and density among healthy AA (HbAnormal) and AC (HbC-trait) subjects were equivalent. [2][3][4][5] Subsequent work failed to associate HbC with malaria protection 6,7 although one study demonstrated increased survival of AC subjects. 5 Recently, however, 2 epidemiologic studies performed in Sahelian regions of West Africa demonstrated the malariaprotective effect of HbC.…”
Section: Introductionmentioning
confidence: 99%
“…1 Early studies found that parasite prevalence and density among healthy AA (HbAnormal) and AC (HbC-trait) subjects were equivalent. [2][3][4][5] Subsequent work failed to associate HbC with malaria protection 6,7 although one study demonstrated increased survival of AC subjects. 5 Recently, however, 2 epidemiologic studies performed in Sahelian regions of West Africa demonstrated the malariaprotective effect of HbC.…”
Section: Introductionmentioning
confidence: 99%
“…20,21 Since the mortality from falciparum malaria was related to parasite densities, 22 these children had a lower mortality rate from malaria. [23][24][25][26] Similar protection is provided by the G-6-PD deficiency, 27,28 and thus an increased frequency of these genes is encountered in most of the areas of the world that are or have been malaria endemic.…”
mentioning
confidence: 99%
“…Sickle Cell-Hemoglobin C Disease -inheritance of the gene for HbS from one parent and the gene for HbC from the other results in sickle cell-hemoglobin C (SC) disease. HbC occurs at high prevalence in Ghana and Burkina Faso 14,15 and is confined to people of West African ancestry, this limited geographical distribution suggesting that the HbC mutation occurred even more recently than HbS. As HbC identifies West African ancestry, SC disease occurs in black populations in North and South America, the Caribbean and Europe but is not seen elsewhere in Africa, around the Mediterranean, Saudi Arabia, or India.…”
Section: Genotype Of Sickle Cell Diseasementioning
confidence: 99%