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Plasmodium falciparum

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Plas·mo·di·um fal·cip·a·rum

Laverania falcipara, a species that is the causal agent of falciparum (malignant tertian) malaria; a young trophozoite is about one fifth the size of an erythrocyte, but developing erythrocytic stages are rarely seen in circulating blood, because they render infected cells sticky and cause them to concentrate in capillaries in the vital organs, particularly the brain and the heart; a schizont occupies about one half to two thirds of the erythrocyte and has fine, sparse granules (observed in peripheral blood only from moribund patients); infected erythrocytes are normal or contracted in size and are likely to contain basophilic granules and red dots (Maurer clefts or dots); multiple infection is extremely frequent, which causes bouts of fever somewhat irregularly, bcause the parasite's cycles of multiplication are usually asynchronous.
Farlex Partner Medical Dictionary © Farlex 2012

Plas·mo·di·um fal·cip·a·rum

(plaz-mōdē-ŭm falsi-pārŭm)
Laverania falciparum, a protozoal species that is the causal agent of falciparum (malignant tertian) malaria; the species is not selective, infecting erythrocytes regardless of whether they are mature or immature or whether they are of normal, large, or contracted size; infected erythrocytes are likely to contain basophilic granules and red dots (Maurer clefts or dots); multiple infection is extremely frequent and causes bouts of fever somewhat irregularly because the parasites' cycles of multiplication are usually asynchronous.
Medical Dictionary for the Health Professions and Nursing © Farlex 2012

Plas·mo·di·um fal·cip·a·rum

(plaz-mōdē-ŭm falsi-pārŭm)
Laverania falcipara, a species that is the causal agent of falciparum (malignant tertian) malaria.
Medical Dictionary for the Dental Professions © Farlex 2012
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References in periodicals archive
Population dynamics of untreated Plasmodium falciparum malaria within the adult human host during the expansion phase of the infection.
Goka et al., "Distinct patterns of cytokine regulation in discrete clinical forms of Plasmodium falciparum malaria," European Cytokine Network, vol.
(iii) Test was considered to be mixed infection if one line appear in the control region, one in the plasmodium falciparum region and one in the pan malarial region.
The heterozygous genotype showed no significant effect in modulating the probability of acquisition of malaria caused by Plasmodium falciparum (OR: 1.343; 95% CI: 0.556 -3.241).
Serum antibodies from malaria-exposed people recognize conserved epitopes formed by the two epidermal grow factors motifs of MSP1(19), the carboxy-terminal fragment of the major merozoite surface protein of Plasmodium falciparum. Infect Immun 1995; 63(2):456-66.
of patients with plasmodium falciparum species infection is 68.57% (n=48), plasmodium vivax species infection is 28.57% (n=20), and total no of mixed infection is 2.857% (n=2).
Plasmodium falciparum is the most lethal amongst all Plasmodium species.
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