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Congenital toxoplasmosis

Definition

Congenital toxoplasmosis is a group of symptoms that occur when an unborn baby (fetus) is infected with the parasite Toxoplasma gondii.

Causes, incidence, and risk factors

The fetus can become infected with toxoplasmosis if the mother becomes infected with toxoplasmosis during the pregnancy. The infection may spread to the fetus during the pregnancy itself, or during labor or delivery.

For the mother, the toxoplasmosis infection is generally mild, and she may not be aware of it. Infection of the fetus, however, can cause severe problems. Infection early in pregnancy results in more severe problems than later infection.

Symptoms

Up to half of the fetuses who become infected with toxoplasmosis during the pregnancy ae born early (prematurely). Congenital toxoplasmosis can damage the baby's eyes, nervous system, skin, and ears.

Often, there are signs of infection in the baby at birth. However, newborns with milder infections may not have symptoms or problems for months or even years. If they are not treated, almost all develop problems (especially in the eyes) when they become adolescents.

Symptoms may include:

Brain and nervous system damage may be severe or very mild, and may include:

  • Seizures
  • Abnormal brain and nervous system (neurologic) function

Signs and tests

The physical examination may show signs of:

Signs and symptoms that occur late in the disease include:

Prenatal tests include:

Postnatal diagnosis:

Congenital Toxoplasmosis Images


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