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Congenital cytomegalovirus is a group of symptoms that occur when an infant is infected with the cytomegalovirus (CMV) before birth. Causes Congenital cytomegalovirus occurs when an infected mother passes CMV to the fetus through the placenta. Treatment is meant to control the infection and relieve symptoms. Medicines to fight the virus (antiviral medications) are prescribed. In people with a healthy immune system, symptoms go away without treatment in most cases. Symptoms are more severe in those with a weakened immune system. There is a high risk of CMV infection in people who receive an organ transplant from a CMV-positive donor. The mother's illness may not have symptoms, so she may be unaware that she has CMV. Symptoms Most congenitally infected children do not have symptoms.


The outcome depends on how severe the immune system deficiency and the CMV infection are. People with AIDS may have a worse outcome than those with a weakened immune system due to another reason.
Gastrointestinal and hepatic complications of solid organ and hematopoietic cell transplantation. The most commonly used medicines are ganciclovir and valganciclovir. In some cases, long-term therapy may be needed. It is spread by saliva, urine, respiratory droplets, sexual contact, and blood transfusions. That way, any growth and development problems can be identified early, and treated promptly. Prevention Cytomegalovirus is almost everywhere in the environment.


Lehrer, MD, Department of Gastroenterology, Frankford-Torresdale Hospital, Aria Health System, Philadelphia, PA.



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