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Published on: July 6, 2013
American Cochlear Implant Alliance Position Statement on Newborn Congenital Cytomegalovirus Screening
Megan Honor Pesch1,2, Kevin David Brown3,4, Amy L Birath4,5
1Division of Developmental and Behavioral Pediatrics, Department of Pediatrics, University of Michigan School of Medicine, Ann Arbor, Michigan, USA.
None:
It is estimated that 1 in every 200 US newborns has congenital cytomegalovirus (cCMV). Delayed identification of cCMV in newborns precludes timely intervention to mitigate sequelae of the infection such as hearing loss and other neurological complications. Newborn testing for cCMV enables appropriate diagnosis and intervention by multidisciplinary teams to properly manage the immediate sequelae of cCMV, avoid unnecessary additional testing that can result from delayed diagnosis, and monitor for future complications. It is the position of the American Cochlear Implant Alliance, the National CMV Foundation, and the American Academy of Otolaryngology-Head and Neck Surgery that universal newborn cCMV screening is necessary to best accomplish these goals.
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