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Valganciclovir for Symptomatic Congenital Cytomegalovirus Disease
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Valganciclovir for Symptomatic Congenital Cytomegalovirus Disease
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Valganciclovir for Symptomatic Congenital Cytomegalovirus Disease
Valganciclovir for Symptomatic Congenital Cytomegalovirus Disease
Journal Article

Valganciclovir for Symptomatic Congenital Cytomegalovirus Disease

2015
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Overview
Cytomegalovirus is an important cause of disease in the newborn. The authors report data from a randomized trial of an extension of valganciclovir therapy from 6 weeks to 6 months for symptomatic CMV disease in newborns. Congenital cytomegalovirus (CMV) infection is the leading nongenetic cause of sensorineural hearing loss 1 – 4 and is the most frequent known viral cause of mental retardation 5 ; the infection affects 0.6 to 0.7% of live births in industrialized countries. 6 – 8 A total of 10% of congenitally infected neonates have symptomatic disease at birth, of whom 35% have sensorineural hearing loss, up to two thirds have neurologic deficits, and 4% die during the newborn period. 7 – 11 Although congenital CMV infection is rare overall, it accounts for 21% of children with hearing loss at birth and 24% of those with hearing loss at . . .