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Universal neonatal hearing screening: Six years of experience in Qatar.

作者信息

Abdul Hadi K, Salahaldin A, Al Qahtani A, Al Musleh Z, Al Sulaitin M, Bener A, Chandra P, Alawi F

机构信息

Hamad Medical Corporation Doha, Qatar.

出版信息

Qatar Med J. 2013 Nov 1;2012(2):42-50. doi: 10.5339/qmj.2012.2.12. eCollection 2012.

DOI:10.5339/qmj.2012.2.12
PMID:25003040
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3991045/
Abstract
摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ad70/3991045/80bd818c7d76/qmj-2012-042-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ad70/3991045/be53d6be7a2f/qmj-2012-042-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ad70/3991045/5d618074fbb3/qmj-2012-042-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ad70/3991045/80bd818c7d76/qmj-2012-042-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ad70/3991045/be53d6be7a2f/qmj-2012-042-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ad70/3991045/5d618074fbb3/qmj-2012-042-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ad70/3991045/80bd818c7d76/qmj-2012-042-g003.jpg

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Frequency of c.35delG Mutation in Gene (Connexin 26) in Syrian Patients with Nonsyndromic Hearing Impairment.

本文引用的文献

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GJB2 and GJB6 genes and the A1555G mitochondrial mutation are only minor causes of nonsyndromic hearing loss in the Qatari population.GJB2 和 GJB6 基因及 A1555G 线粒体突变仅为卡塔尔人群中非综合征性听力损失的次要原因。
Int J Audiol. 2012 Mar;51(3):181-5. doi: 10.3109/14992027.2011.625983. Epub 2011 Nov 21.
2
Newborn hearing assessment in 2010.2010年新生儿听力评估
Med Health R I. 2010 May;93(5):142-4.
3
Evaluating loss to follow-up in newborn hearing screening in Massachusetts.评估马萨诸塞州新生儿听力筛查中的失访情况。
叙利亚非综合征性听力损失患者中基因（连接蛋白26）c.35delG突变的频率
Genet Res Int. 2017;2017:5836525. doi: 10.1155/2017/5836525. Epub 2017 Dec 6.
4
Risk factors for hearing loss in infants under universal hearing screening program in Northern Thailand.泰国北部全民听力筛查项目下婴儿听力损失的风险因素
J Multidiscip Healthc. 2015 Dec 24;9:1-5. doi: 10.2147/JMDH.S92818. eCollection 2016.
Pediatrics. 2008 Feb;121(2):e335-43. doi: 10.1542/peds.2006-3540. Epub 2008 Jan 10.
4
Year 2007 position statement: Principles and guidelines for early hearing detection and intervention programs.2007年立场声明：早期听力检测与干预项目的原则和指南
Pediatrics. 2007 Oct;120(4):898-921. doi: 10.1542/peds.2007-2333.
5
Universal newborn hearing screening: are we achieving the Joint Committee on Infant Hearing (JCIH) objectives?新生儿听力普遍筛查：我们是否实现了婴儿听力联合委员会（JCIH）的目标？
Laryngoscope. 2005 Feb;115(2):232-6. doi: 10.1097/01.mlg.0000154724.00787.49.
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From Screening to Early Identification and Intervention: Discovering Predictors to Successful Outcomes for Children With Significant Hearing Loss.从筛查到早期识别与干预：探寻重度听力损失儿童成功康复的预测因素
J Deaf Stud Deaf Educ. 2003 Winter;8(1):11-30. doi: 10.1093/deafed/8.1.11.
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Arch Dis Child Fetal Neonatal Ed. 2004 Sep;89(5):F378-83. doi: 10.1136/adc.2003.034454.
8
Newborn hearing screening: recommendations and rationale.新生儿听力筛查：建议与依据。
Am Fam Physician. 2001 Dec 15;64(12):1995-9.
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Prevalence of permanent childhood hearing impairment in the United Kingdom and implications for universal neonatal hearing screening: questionnaire based ascertainment study.英国儿童永久性听力障碍的患病率及其对新生儿普遍听力筛查的影响：基于问卷调查的确定研究
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