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congenital toxoplasmosis |
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congenital toxoplasmosis
A transplacental infection with the protozoan Toxoplasma gondii affecting ±1⁄3 of fetuses of ♀ with acute acquired toxoplasmosis, most severe if the infection occurs in
1st trimester; children are often normal at birth, followed by blindness, mental retardation; it may affect the brain, lung, heart, eyes, liver Clinical Hydrocephalus, microcephaly, cerebral calcifications, atrophy, chorioretinitis,
uveitis, vitritis, convulsions, hyperbilirubinemia, hepatomegaly Diagnosis PCR of amniotic fluid to detect 35-fold repeat of the B1 gene of T gondii Sensitivity 97%–vs 90% with conventional parasitology Lab IgM immunoassay
Management Pyrimethamine, sulfadiazine, leukovorin. See TORCH. Want to thank TFD for its existence? Tell a friend about us, add a link to this page, add the site to iGoogle, or visit the webmaster's page for free fun content. |
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