Congenital malaria: Difference between revisions
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Latest revision as of 16:51, 22 March 2025
Congenital Malaria is a malaria infection transmitted from a mother to her offspring during childbirth. This condition is a significant health concern in areas where malaria is endemic, such as Sub-Saharan Africa, Southeast Asia, and South America.
Etiology[edit]
Congenital malaria is caused by the Plasmodium species, which includes Plasmodium falciparum, Plasmodium vivax, Plasmodium ovale, and Plasmodium malariae. These parasites are transmitted from the infected mother to the newborn during delivery.
Symptoms[edit]
The symptoms of congenital malaria can appear within a few days to several weeks after birth. They may include fever, irritability, feeding problems, anemia, and an enlarged spleen or liver.
Diagnosis[edit]
Diagnosis of congenital malaria is made by identifying the Plasmodium parasites in a blood sample. This can be done using a microscopic examination of a blood smear or a rapid diagnostic test.
Treatment[edit]
Treatment for congenital malaria involves the use of antimalarial drugs. The choice of drug depends on the species of Plasmodium causing the infection and the drug resistance patterns in the area where the infection was acquired.
Prevention[edit]
Prevention of congenital malaria involves preventing malaria in pregnant women through the use of insecticide-treated nets, intermittent preventive treatment during pregnancy, and prompt treatment of malaria infections.
