In the "at-risk" population that figure is 30 to 60 times higher than in the general population. "At-risk" children are those who have other identifiable disabilities or who may be susceptible due to premature birth.Testing for Hearing Loss in ChildrenHilt, Gary...
The only parents who changed their views regarding the usefulness of genetic testing for hearing loss were those who reported that their children underwent significant changes in their hearing loss or were faced with other life threatening conditions. Parents were also often unaware of the role of ...
Ji et al., "Genetic testing for sporadic hearing loss using targeted massively parallel sequencing identifies 10 novel mutations," Clinical Genetics, vol. 87, no. 6, pp. 588-593, 2015.Gu X, Guo L, Ji H, Sun S, Chai R, Wang L, Li H. Genetic testing for sporadic hearing loss using...
Embarking on any new journey can feel daunting, and getting treatment forhearing lossis no exception. You might not know where to start, but an audiologist can guide you through the process of getting your hearing tested. Once you have those results, you and the team at Southwestern Hearing ...
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Hearing loss is the most common sensory disorder in children, with an incidence of 1 in 500 newborns. Most cases are caused by mutations in a single gene. ... M Sommen,GV Camp - 《B Ent》 被引量: 8发表: 2013年 The next-generation sequencing analysis for hereditary hearing loss Recent...
The conclusion is that refreshment training with fit testing, continuous focus on hearing loss prevention, and having an adequate selection of hearing protection device styles and sizes, are crucial for ensuring the proposer's use of appropriate hearing protection and preventing occupational NIHL. ...
newborn for a specific genetic variant using blood sample, for certain genetic, endocrine, and metabolic disorders, and are also tested for hearing loss and critical congenital heart defects [CCHDs] All states must screen for at least 21 disorders by law, and some states test for 30 or...
An abstract is unavailable.doi:10.1097/01.HJ.0000414381.05364.90R.L. MartinC.W. AspHearing Journal
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