Diagnosis and management of conductive hearing loss in children with trisomy 21
Author:
Affiliation:
1. Department of Otolaryngology; Craigavon Area Hospital; Craigavon Northern Ireland
Publisher
Wiley
Subject
Pediatrics, Perinatology, and Child Health
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/jpc.14065/fullpdf
Reference11 articles.
1. Trends in Down's syndrome live births and antenatal diagnoses in England and Wales from 1989 to 2008: Analysis of data from the National Down Syndrome Cytogenetic Register;Morris;BMJ,2009
2. Mortality associated with Down's syndrome in the USA from 1983 to 1997: A population based study;Yang;Lancet,2002
3. Primary ciliary dyskinesia associated with a novel microtubule defect in a child with Down's syndrome;Kovesi;Chest,2000
4. Prevalence and nature of hearing loss in 22q11.2 deletion syndrome;Van Eynde;J. Speech Lang. Hear. Res.,2016
5. Hearing in school-aged children with trisomy 21 - Results of a longitudinal cohort study in children identified at birth;Yaneza;Clin. Otolaryngol.,2016
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1. Conductive hearing loss in newborns: Hearing profile, risk factors, and occasions of service;International Journal of Pediatric Otorhinolaryngology;2023-08
2. Characterisation of the treatment provided for children with unilateral hearing loss;Frontiers in Pediatrics;2023-07-25
3. Toward Optimal Care for Children With Congenital Unilateral Aural Atresia;Frontiers in Neurology;2021-07-08
4. Contribution of spectral pinna cues for sound localization in children with congenital unilateral conductive hearing loss after hearing rehabilitation;Hearing Research;2020-01
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