Congenital toxoplasmosis (Q45777): Difference between revisions
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Doença causada por uma infecção pelo parasita protozoário Toxoplasma gondii no útero. Esta doença é caracterizada por coriorretinite, hidrocefalia, calcificações intracranianas, anemia ou déficits neurológicos que se desenvolvem após o nascimento. Esta doença pode se manifestar ao nascimento com icterícia, parto prematuro, hepatoesplenomegalia, miocardite, pneumonite ou erupção cutânea. A transmissão ocorre por transmissão vertical. No feto, a confirmação é feita pela identificação de Toxoplasma gondii no líquido amniótico; no recém-nascido, a confirmação se dá pela identificação de Toxoplasma gondii em fluidos ou tecidos corporais, ou detecção de anticorpos contra Toxoplasma gondii. | |||
| description / en | description / en | ||
A disease caused by an infection with the protozoan parasite Toxoplasma gondii in utero. This disease is characterised by chorioretinitis, hydrocephalus, intracranial calcifications, anaemia, or neurological deficits that develop after birth. This disease may present at birth with jaundice, premature birth, hepatosplenomegaly, myocarditis, pneumonitis, or rash. Transmission is by vertical transmission. In the fetus, confirmation is by identification of Toxoplasma gondii in amniotic fluid; in the neonate, confirmation is by identification of Toxoplasma gondii in body fluids or tissues, or detection of antibodies against Toxoplasma gondii. | |||
Revision as of 13:58, 13 August 2026
A disease caused by an infection with the protozoan parasite Toxoplasma gondii in utero. This disease is characterised by chorioretinitis, hydrocephalus, intracranial calcifications, anaemia, or neurological deficits that develop after birth. This disease may present at birth with jaundice, premature birth, hepatosplenomegaly, myocarditis, pneumonitis, or rash. Transmission is by vertical transmission. In the fetus, confirmation is by identification of Toxoplasma gondii in amniotic fluid; in the neonate, confirmation is by identification of Toxoplasma gondii in body fluids or tissues, or detection of antibodies against Toxoplasma gondii.
| Language | Label | Description | Also known as |
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| default for all languages | KA64.0 |
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| English | Congenital toxoplasmosis |
A disease caused by an infection with the protozoan parasite Toxoplasma gondii in utero. This disease is characterised by chorioretinitis, hydrocephalus, intracranial calcifications, anaemia, or neurological deficits that develop after birth. This disease may present at birth with jaundice, premature birth, hepatosplenomegaly, myocarditis, pneumonitis, or rash. Transmission is by vertical transmission. In the fetus, confirmation is by identification of Toxoplasma gondii in amniotic fluid; in the neonate, confirmation is by identification of Toxoplasma gondii in body fluids or tissues, or detection of antibodies against Toxoplasma gondii. |
