Show simple item record

dc.contributor.authorOkeyo, Winnie A
dc.contributor.authorMunde, Elly O
dc.contributor.authorOkumu, Wilson
dc.contributor.authorRaballah, Evans
dc.contributor.authorAnyona, Samuel B
dc.contributor.authorVulule, John M
dc.contributor.authorOng’echa, John M
dc.contributor.authorPerkins, Douglas J
dc.contributor.authorOuma, Collins
dc.date.accessioned2018-01-23T10:12:06Z
dc.date.available2018-01-23T10:12:06Z
dc.date.issued2013
dc.identifier.urihttps://repository.maseno.ac.ke/handle/123456789/189
dc.description.abstractIn holoendemic Plasmodium falciparum transmission areas such as western Kenya, severe malarial anemia [SMA, hemoglobin (Hb)< 6.0 g/dL, with any density parasitemia] is the most common clinical manifestation of severe malaria resulting in high rates of pediatric morbidity and mortality in these regions. Previous studies associated interleukin (IL)-13 with pathogenesis of different infectious diseases, including P. falciparum malaria. However, the functional roles of polymorphic variants within the IL-13 promoter in conditioning susceptibility to SMA remain largely unexplored. As such, the association between the IL-13 variants-7402 T/G (rs7719175) and-4729G/A (rs3091307) and susceptibility to SMA was determined in children (n= 387) presenting with clinical symptoms of falciparum malaria and resident in a holoendemic transmission region in western Kenya. Our results indicated no …en_US
dc.publisherBio Med Centralen_US
dc.title(− 7402 T/G and-4729G/A) condition susceptibility to pediatric severe malarial anemia but not circulating IL-13 levelsen_US
dc.typeArticleen_US


Files in this item

Thumbnail

This item appears in the following Collection(s)

Show simple item record