Congenital rubella – Symptoms, Diagnosis, Treatment, Prevention

Congenital rubella is a condition that occurs when a pregnant woman is infected with the rubella virus, also known as German measles, and passes the infection to her baby. Congenital rubella can cause a range of birth defects and other health problems in the newborn. In this article, we will explore the symptoms, diagnosis, treatment, and prevention of congenital rubella.

Symptoms of congenital rubella

Symptoms of congenital rubella vary that include:

• Birth defects, including heart defects, hearing loss, and eye problems
• Developmental delays
• Seizures
• Small head size (microcephaly)
• Purple skin patches (purpura)
• Enlarged liver and spleen (hepatosplenomegaly)

Symptoms may not appear until several months after birth. In severe cases, congenital rubella can be fatal.

Diagnosis of congenital rubella

Congenital rubella is typically diagnosed based on the presence of characteristic symptoms and a history of the mother being infected with rubella during pregnancy. Laboratory blood tests are also used to confirm the diagnosis.

Treatment of congenital rubella

There is no specific treatment for congenital rubella. Treatment is typically supportive that includes measures to manage symptoms and address any birth defects or other health problems.

Prevention of congenital rubella

Congenital rubella can be prevented through vaccination. The rubella vaccine is typically given as part of the measles, mumps, and rubella (MMR) vaccine.

It is important for women who are planning to become pregnant to ensure that they are up to date on their vaccinations, including the MMR vaccine. Women who are pregnant or planning to become pregnant should also avoid contact with individuals who have rubella or are experiencing rubella-like symptoms.

It is important to seek medical attention if congenital rubella is suspected, as early treatment can help to manage symptoms and reduce the risk of complications.