Literature DB >> 10626584

The need for universal neonatal hearing screening--some aspects of epidemiology and identification.

A Parving1.   

Abstract

The devastating consequences of a congenital/early-acquired hearing disability on the speech language and social development of a child and the estimated prevalence rates of at least 1-1.5/1000 live births of congenital permanent hearing impairment are important health problems. Universal neonatal hearing screening programs have provided the opportunity to detect neonates with permanent congenital hearing loss, and thus initiate auditory rehabilitation before the age of 3 mo. Universal neonatal hearing screening represents secondary prevention of hearing impairment/deafness, and the world-wide documented delayed identification of children with congenital/early-acquired hearing impairment will no doubt be improved with the implementation of universal neonatal hearing screening programs.

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Mesh:

Year:  1999        PMID: 10626584     DOI: 10.1111/j.1651-2227.1999.tb01163.x

Source DB:  PubMed          Journal:  Acta Paediatr Suppl        ISSN: 0803-5326


  13 in total

1.  Cranial Nerve VIII: Hearing and Vestibular Functions.

Authors:  Richard D Sanders; Paulette Marie Gillig
Journal:  Psychiatry (Edgmont)       Date:  2010-03

2.  In search of genetic markers for nonsyndromic deafness in Africa: a study in Cameroonians and Black South Africans with the GJB6 and GJA1 candidate genes.

Authors:  Jason Bosch; Kamogelo Lebeko; Jean Jacques Noubiap Nziale; Collet Dandara; Nomlindo Makubalo; Ambroise Wonkam
Journal:  OMICS       Date:  2014-05-02

Review 3.  Hereditary non-syndromic sensorineural hearing loss: transforming silence to sound.

Authors:  Iris Schrijver
Journal:  J Mol Diagn       Date:  2004-11       Impact factor: 5.568

Review 4.  Early detection of hearing impairment in newborns and infants.

Authors:  Martin Ptok
Journal:  Dtsch Arztebl Int       Date:  2011-06-24       Impact factor: 5.594

5.  Effectiveness of a TEOAE-based screening program. Can a patient-tracking system effectively be organized using modern information technology and central data management?

Authors:  W Delb; D Merkel; K Pilorget; J Schmitt; P K Plinkert
Journal:  Eur Arch Otorhinolaryngol       Date:  2003-08-28       Impact factor: 2.503

Review 6.  Human hereditary hearing impairment: mouse models can help to solve the puzzle.

Authors:  Karen Vrijens; Lut Van Laer; Guy Van Camp
Journal:  Hum Genet       Date:  2008-09-11       Impact factor: 4.132

7.  Mutation analysis of TMC1 identifies four new mutations and suggests an additional deafness gene at loci DFNA36 and DFNB7/11.

Authors:  N Hilgert; F Alasti; N Dieltjens; B Pawlik; B Wollnik; O Uyguner; S Delmaghani; D Weil; C Petit; E Danis; T Yang; E Pandelia; M B Petersen; D Goossens; J D Favero; M H Sanati; R J H Smith; G Van Camp
Journal:  Clin Genet       Date:  2008-07-09       Impact factor: 4.438

8.  Myosin light-chain kinase is necessary for membrane homeostasis in cochlear inner hair cells.

Authors:  Guang-Jie Zhu; Fang Wang; Chen Chen; Lin Xu; Wen-Cheng Zhang; Chi Fan; Ya-Jing Peng; Jie Chen; Wei-Qi He; Shi-Ying Guo; Jian Zuo; Xia Gao; Min-Sheng Zhu
Journal:  PLoS One       Date:  2012-04-02       Impact factor: 3.240

9.  Screening of deafness-causing DNA variants that are common in patients of European ancestry using a microarray-based approach.

Authors:  Denise Yan; Guangxin Xiang; Xingping Chai; Jie Qing; Haiqiong Shang; Bing Zou; Rahul Mittal; Jun Shen; Richard J H Smith; Yao-Shan Fan; Susan H Blanton; Mustafa Tekin; Cynthia Morton; Wanli Xing; Jing Cheng; Xue Zhong Liu
Journal:  PLoS One       Date:  2017-03-08       Impact factor: 3.240

10.  Over-expression of myosin7A in cochlear hair cells of circling mice.

Authors:  Yoo Yeon Kim; Hajin Nam; Harry Jung; Boyoung Kim; Jun Gyo Suh
Journal:  Lab Anim Res       Date:  2017-03-27
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