Congenital cytomegalovirus

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Congenital cytomagalovirus

Congenital cytomegalovirus

Definition:

Congenital cytomegalovirus is a cluster of findings associated with infection of the fetus by cytomegalovirus (CMV).

Alternative Names:

CMV - congenital; Congenital CMV

Causes, incidence, and risk factors:

Congenital cytomegalovirus is caused when an infected mother passes CMV to the fetus through the placenta. The mother's illness may be subclinical (without symptoms, asymptomatic), and she may be unaware that any problems exist.

The majority of congenitally infected children are asymptomatic. The symptomatic infant is characteristically born with a petechial rash (a rash that looks like fine purplish-colored dots), a large spleen and liver, jaundice, inflammation of the retina, intracranial calcifications (mineral deposits within the brain), and a small head (microcephaly).

Only about 1 out of 10 infants congenitally infected with CMV are thought to exhibit these symptoms.

Review Date: 12/1/2005
Reviewed By: Daniel Rauch, MD, FAAP, Director, Pediatric Hospitalist Program, Associate Professor of Pediatrics, NYU School of Medicine, New York, NY. Review provided by VeriMed Healthcare Network.

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