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Rash
Jaundice (yellowing of the skin or
whites of the eyes)
Microcephaly (small head)
Low birth weight
Hepatosplenomegaly (enlarged
liver and spleen)
Seizures
Retinitis (damaged eye retina)
Hearing loss
Developmental and motor delay
Vision loss
Microcephaly (small head)
Seizures
Some babies can have hearing loss at birth or can develop it later, even babies who passed the newborn hearing test or
didn’t have any other sings at birth.
CMV is the most common infectious cause of birth defects in the United States. About 1 out of 200 babies is born
with congenital CMV.
One out of 5 babies with congenital CMV will have symptoms or long-term health problems, such as hearing loss.
Parents and childcare providers can lower their risk of getting CMV by reducing contact with saliva (spit) and urine from
babies and young children.
Diagnosis
Congenital CMV infection can be diagnosed by testing a newborn baby’s urine (preferred specimen), saliva, or blood.
These specimens must be collected for testing within 2 to 3 weeks after the baby is born to confirm a diagnosis of
congenital CMV infection.
Treatment
For babies with signs of congenital CMV infection at birth, antiviral medications (primarily valganciclovir) might improve
hearing and developmental outcomes. Valganciclovir can have serious side effects and has only been studied in babies
with signs of congenital CMV infection. There is limited information on the effectiveness of valganciclovir to treat infants
with hearing loss alone.
https://www.cdc.gov/cmv/congenital-infection.html 2/2