Newborn Hearing Screening — A Silent Revolution
The implementation of universal screening programs to detect hearing defects in newborns has dramatically increased the identification of hearing loss in infants. Recent advances in understanding the nature and causes of prelingual hearing loss, combined with advances in technology, suggest that fur...
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| Published in | The New England journal of medicine Vol. 354; no. 20; pp. 2151 - 2164 |
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| Main Authors | , |
| Format | Journal Article |
| Language | English |
| Published |
Boston, MA
Massachusetts Medical Society
18.05.2006
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| Subjects | |
| Online Access | Get full text |
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| Abstract | The implementation of universal screening programs to detect hearing defects in newborns has dramatically increased the identification of hearing loss in infants. Recent advances in understanding the nature and causes of prelingual hearing loss, combined with advances in technology, suggest that further improvement in these programs can readily be achieved.
Recent advances in understanding the nature and causes of prelingual hearing loss, combined with advances in technology, suggest that further improvement in screening programs can readily be achieved.
Hearing loss is an etiologically heterogeneous trait with many known genetic and environmental causes.
1
Historically, some environmental causes of hearing loss, such as rubella embryopathy, have been epidemic in nature, establishing that the incidence of congenital deafness can vary widely at various times and among populations. Other important environmental causes of hearing loss include prematurity, prenatal and postnatal infections, head trauma, subarachnoid hemorrhage, and pharmacologic ototoxicity. Genetic causes account for at least 50 to 60 percent of childhood hearing loss in developed countries and can be classified according to the pattern of inheritance, the presence (syndromic) or absence (nonsyndromic) of . . . |
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| AbstractList | The implementation of universal screening programs to detect hearing defects in newborns has dramatically increased the identification of hearing loss in infants. Recent advances in understanding the nature and causes of prelingual hearing loss, combined with advances in technology, suggest that further improvement in these programs can readily be achieved.
Recent advances in understanding the nature and causes of prelingual hearing loss, combined with advances in technology, suggest that further improvement in screening programs can readily be achieved.
Hearing loss is an etiologically heterogeneous trait with many known genetic and environmental causes.
1
Historically, some environmental causes of hearing loss, such as rubella embryopathy, have been epidemic in nature, establishing that the incidence of congenital deafness can vary widely at various times and among populations. Other important environmental causes of hearing loss include prematurity, prenatal and postnatal infections, head trauma, subarachnoid hemorrhage, and pharmacologic ototoxicity. Genetic causes account for at least 50 to 60 percent of childhood hearing loss in developed countries and can be classified according to the pattern of inheritance, the presence (syndromic) or absence (nonsyndromic) of . . . The implementation of universal screening programs to detect hearing defects in newborns has dramatically increased the identification of hearing loss in infants. Recent advances in understanding the nature and causes of prelingual hearing loss, combined with advances in technology, suggest that further improvement in these programs can readily be achieved. |
| Author | Morton, Cynthia C Nance, Walter E |
| Author_xml | – sequence: 1 givenname: Cynthia C surname: Morton fullname: Morton, Cynthia C – sequence: 2 givenname: Walter E surname: Nance fullname: Nance, Walter E |
| BackLink | http://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=17767925$$DView record in Pascal Francis https://www.ncbi.nlm.nih.gov/pubmed/16707752$$D View this record in MEDLINE/PubMed |
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| Copyright | Copyright © 2006 Massachusetts Medical Society. All rights reserved. 2006 INIST-CNRS |
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| References_xml | – volume: 36 start-page: 829 year: 1999 ident: r031 publication-title: J Med Genet – ident: r043 doi: 10.1097/01.GIM.0000144187.21727.28 – ident: r011 doi: 10.1136/adc.2003.034454 – ident: r010 doi: 10.1542/peds.102.5.1161 – ident: r037 doi: 10.1097/00006454-200301000-00012 – ident: r042 doi: 10.1136/jmg.40.8.632 – ident: r022 doi: 10.1542/peds.2004-1688 – ident: r033 doi: 10.1097/01.GIM.0000078026.01140.68 – ident: r015 doi: 10.1097/01.AUD.0000051749.40991.1F – ident: r041 doi: 10.1016/S0196-0709(97)90078-8 – ident: r027 doi: 10.1242/dev.00376 – ident: r028 doi: 10.1016/j.otohns.2004.06.707 – ident: r030 doi: 10.1002/cne.10916 – volume: 14 start-page: 18 year: 1993 ident: r005 publication-title: Semin Hearing – ident: r044 doi: 10.1001/archotol.130.5.634 – ident: r045 doi: 10.1038/nm1193 – ident: r024 doi: 10.1093/qjmed/90.7.443 – ident: r025 doi: 10.1002/humu.1116 – ident: r039 doi: 10.1016/S0022-3476(97)70248-8 – ident: r016 doi: 10.1002/mrdd.10088 – ident: r008 doi: 10.1542/peds.109.1.e7 – ident: r026 doi: 10.1136/jmg.2004.024208 – ident: r029 doi: 10.1016/S0140-6736(98)11071-1 – ident: r013 doi: 10.1016/j.jcv.2005.09.017 – ident: r007 doi: 10.1016/0165-5876(95)01183-C – ident: r023 doi: 10.1093/oso/9780195138498.001.0001 – ident: r032 doi: 10.1136/jmg.2003.013896 – ident: r035 doi: 10.1016/S0140-6736(00)02565-4 – ident: r038 doi: 10.1136/adc.62.12.1233 – ident: r046 doi: 10.1097/00125817-200205000-00011 – ident: r036 doi: 10.1086/420979 – volume: 4 start-page: 69 year: 1964 ident: r002 publication-title: J Aud Res – ident: r012 doi: 10.1136/bmj.323.7312.536 – volume: 74 start-page: 1208 year: 1970 ident: r003 publication-title: Trans Am Acad Ophthalmol Otolaryngol – ident: r020 doi: 10.1016/0165-5876(89)90062-1 – ident: r009 doi: 10.1002/mrdd.10061 – volume: 56 start-page: 352 year: 1997 ident: r006 publication-title: Hawaii Med J – ident: r040 doi: 10.1016/S0022-3476(99)70328-8 – ident: r017 doi: 10.1002/mrdd.10063 – ident: r001 doi: 10.1002/mrdd.10067 – ident: r004 doi: 10.1002/mrdd.10082 – ident: r034 doi: 10.1136/jmg.38.8.515 – ident: r047 doi: 10.1126/science.311.5767.1544 |
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| Snippet | The implementation of universal screening programs to detect hearing defects in newborns has dramatically increased the identification of hearing loss in... |
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| SubjectTerms | Biological and medical sciences Children & youth Ear - anatomy & histology Ears & hearing Emissions General aspects Hearing loss Hearing Loss - diagnosis Hearing Loss - etiology Hearing Loss - genetics Hearing Tests Humans Infant, Newborn Medical sciences Neonatal Screening Newborn babies |
| Title | Newborn Hearing Screening — A Silent Revolution |
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