Actualización de los programas de detección precoz de la sordera infantilrecomendaciones CODEPEH 2018 (Nivel 1: Detección)

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• Nuñez-Ramos, R. et al. (2013): “Early diagnosis of congenital cytomegalovirus infection: lost opportunities”. Enferm Infecc Microbiol Clin, 31: 93-96.
• Park, A. H. et al. (2014): “A diagnostic paradigm including cytomegalovirus testing for idiopathic pediatric sensorineural hearing loss”. Laryngoscope, 124: 2624-2629.
• Peng, Q. et al. (2016): “Concurrent genetic and standard screening for hearing impairment in 9317 southern chinese newborns”. Genet Test Mol Biomarkers, 20: 603-608.
• Pimperton, H. et al. (2017): “Language outcomes in deaf or hard of hearing teenagers who are spoken language users: effects of universal newborn hearing screening and early confirmation”. Ear Hear, 38: 598-610.
• Pimperton, H. et al. (2016): “The impact of universal newborn hearing screening on long-term literacy outcomes: a prospective cohort study”. Arch Dis Child, 101: 9-15.
• Pryor, S. P. et al. (2005): “SLC26A4/PDS genotype phenotype correlation in hearing loss with enlargement of the vestibular aqueduct (EVA): evidence that Pendred syndrome and non-syndromic EVA are distinct clinical and genetic entities”. J Med Genet, 42: 159-165.
• Ravi, R. et al. (2016): “Follow-up in newborn hearing screening. A systematic review”. Intl J Pediatr Otorhinolaryngol, 90: 29-36.
• Rawlinson, W. D. et al. (2018): “Neonates with congenital cytomegalovirus and hearing loss identified via the universal newborn hearing screening program”. J ClinVirol, 102: 110-115.
• Rawlinson, W. D. et al. (2017): “Congenital cytomegalovirus infection in pregnancy and the neonate: Consensus recommendations for prevention, diagnosis, and therapy”. Lancet Infect Dis, 17: e177-188.
• Ross, S. A. et al. (2017): “Newborn dried blood spot polymerase chain reaction to identify infants with congenital cytomegalovirus-associated sensorineural hearing loss”. J Pediatr, 184: 57-61.
• Ross, S. A. et al. (2015): “National Institute on Deafness and Other Communication Disorders CHIMES Study. Urine collection method for the diagnosis of congenital cytomegalovirus infection”. Pediatr Infect Dis, 34: 903-905.
• Schimmenti, L. A. et al. (2011): “Evaluation of newborn screening bloodspot-based genetic testing as second tier screen for bedside newborn hearing screening”. Genet Med, 13: 1006-1010.
• Stehel, E. K. et al. (2008): “Newborn hearing screening and detection of congenital cytomegalovirus infection”. Pediatrics, 121: 970-975.
• Smiechura, M. et al. (2014): “Congenital and acquired cytomegalovirus infection and hearing evaluation in children”. Otolaryngol Pol, 68: 303-307.
• Sun, et al. (2015): “Combined hearing and deafness gene mutation screening of 11,046 Chinese newborns”. Zhonghua Yi Xue Yi ChuanXueZaZhi, 32 (6): 766-770.
• Teek, R. et al. (2013): “Hearing impairment in Estonia: an algorithm to investigate genetic causes in pediatric patients”. Adv Med Sci, 58: 419-428.
• Toumpas, C. J. et al. (2015): “Congenital cytomegalovirus infection is a significant cause of moderate to profound sensorineural hearing loss in Queensland children”. J Paediatr Child Health, 51: 541-544.