2020
DOI: 10.1186/s12936-020-03500-5
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Prevalence of sickle cell disorders and malaria infection in children aged 1–12 years in the Volta Region, Ghana: a community-based study

Abstract: Background Alterations in the structure of haemoglobin (Hb) are usually brought about by point mutations affecting one or, in some cases, two codons encoding amino acids of the globin chains. One in three Ghanaians are said to have sickle cell disorders, whereas malaria continues to be one of the leading causes of mortality among children. This study determined the prevalence of sickle cell disorders and malaria infection among children aged 1–12 years in the Volta Region. … Show more

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Cited by 13 publications
(10 citation statements)
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“…falciparum infection did not differ among the three sites, but the median parasite density was significantly higher at Krachi than the two other study sites. Parasite prevalence by PCR (already described in [ 23 ]) was higher than prevalence by microscopy. It did not however differ between the three sites ( Table 1 ).…”
Section: Resultsmentioning
confidence: 99%
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“…falciparum infection did not differ among the three sites, but the median parasite density was significantly higher at Krachi than the two other study sites. Parasite prevalence by PCR (already described in [ 23 ]) was higher than prevalence by microscopy. It did not however differ between the three sites ( Table 1 ).…”
Section: Resultsmentioning
confidence: 99%
“…The study involved children aged 1–12 years living in communities within the selected districts. The study site and population have been described elsewhere [ 23 ]. Briefly, the study employed a multi-stage sampling method in which the three [ 3 ] ecological zones of the Volta Region, southern, middle and northern zones reflecting the three malaria transmission zones, were used.…”
Section: Methodsmentioning
confidence: 99%
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“…All children sampled had no clinical symptoms. The population and sites of the larger study have been described in detail elsewhere (Oppong et al, 2020;Kyei-Baafour et al, 2021).…”
Section: Population and Study Sitesmentioning
confidence: 99%
“…In the tropics, SCD is commonly present in the severe homozygous SS (HbSS), heterozygous SC (HbSC), and the beta-zero or beta-plus thalassemia (HbSβ°/ HbSβ + thalassemia). 1,2 Globally, it is estimated that nearly 5% of the world's population have SCT, and almost 300,000 babies are born with SCD annually. 3,4 Ghana significantly contributes to this global prevalence, with about 2% (approximately 15,000) of all newborns having SCD, and more than half have the severe form of the disease.…”
Section: Introductionmentioning
confidence: 99%