Literature DB >> 20637511

Parental attitudes toward genetic testing for prelingual deafness in China.

Siqing Fu1, Jiashu Dong, Chunfang Wang, Guanming Chen.   

Abstract

OBJECTIVE: Recent advances in molecular biology of hearing and deafness have made genetic testing an option for deaf individuals and their families. In China, DNA microarray and other genetic testing method has been applied to rapid genetic diagnosis of non-syndromic hearing loss. However, there is no information about the interests in such testing in China. The purpose of this study is to document the attitudes of parents with normal hearing who have one or more deaf children toward diagnostic, carrier, and prenatal genetic testing for deafness.
METHODS: A structured, self-completion questionnaire was given to delegates at a conference held at Hubei Rehabilitation Research Center for Deaf Children, Wuhan, China on March 3, 2010. Of 366 surveys distributed, 290 were completed and returned.
RESULTS: Ninety-four percent of the respondents had a positive attitude toward genetic testing. Seventy-two percent stated that they were interested in genetic testing of deaf child. Of the individuals who were interested in such testing, 69% would consider having prenatal genetic testing for deafness.
CONCLUSION: The present study provided evidence of a predominantly positive attitude toward genetics. Appropriate genetic counseling can help parents to understand the risk, benefits, and limitations of genetic testing for prelingual deafness.
Copyright © 2010 Elsevier Ireland Ltd. All rights reserved.

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Year:  2010        PMID: 20637511     DOI: 10.1016/j.ijporl.2010.06.012

Source DB:  PubMed          Journal:  Int J Pediatr Otorhinolaryngol        ISSN: 0165-5876            Impact factor:   1.675


  3 in total

1.  Attitudes Toward Autism Spectrum Disorders Among Students of Allied Health Professions.

Authors:  Frida Simonstein; Michal Mashiach-Eizenberg
Journal:  J Genet Couns       Date:  2016-06-02       Impact factor: 2.537

2.  A quantitative cSMART assay for noninvasive prenatal screening of autosomal recessive nonsyndromic hearing loss caused by GJB2 and SLC26A4 mutations.

Authors:  Mingyu Han; Zhifeng Li; Wenlu Wang; Shasha Huang; Yanping Lu; Zhiying Gao; Longxia Wang; Dongyang Kang; Linwei Li; Yiqian Liu; Mengnan Xu; David S Cram; Pu Dai
Journal:  Genet Med       Date:  2017-05-25       Impact factor: 8.822

3.  'Civilising' Deaf people in Tibet and Inner Mongolia: governing linguistic, ethnic and bodily difference in China.

Authors:  Theresia Hofer; Gry Sagli
Journal:  Disabil Soc       Date:  2017-04-02
  3 in total

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