首页> 外文期刊>American journal of medical genetics, Part A >Do parental perceptions and motivations towards genetic testing and prenatal diagnosis for deafness vary in different cultures?
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Do parental perceptions and motivations towards genetic testing and prenatal diagnosis for deafness vary in different cultures?

机译:不同文化对父母的遗传检测和产前诊断的认知和动机是否不同?

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Surveys of attitudes of individuals with deafness and their families towards genetic testing or prenatal diagnosis have mostly been carried out in the West. It is expected that the perceptions and attitudes would vary amongst persons of different cultures and economic background. There is little information on the prevailing attitudes for genetic testing and prenatal diagnosis for deafness in developing countries. Therefore, this study evaluates the motivations of Indian people with inherited hearing loss towards such testing. Twenty-eight families with history of congenital hearing loss (23 hearing parents with child/family member with deafness, 4 couples with both partners having deafness and 1 parent and child with deafness) participated in a semi-structured survey investigating their interest, attitudes, and intentions for using genetic and prenatal testing for deafness. Participants opinioned that proper management and care of individuals with deafness were handicapped by limited rehabilitation facilities with significant financial and social burden. Nineteen (68%) opted for genetic testing. Twenty-six (93%) expressed high interest in prenatal diagnosis, while 19 (73%) would consider termination of an affected fetus. Three hearing couples, in whom the causative mutations were identified, opted for prenatal diagnosis. On testing, all the three fetuses were affected and the hearing parents elected to terminate the pregnancies. This study provides an insight into the contrasting perceptions towards hearing disability in India and its influence on the desirability of genetic testing and prenatal diagnosis.
机译:聋人及其家属对基因检测或产前诊断的态度调查大部分是在西方进行的。预期不同文化和经济背景的人的看法和态度会有所不同。关于发展中国家对耳聋进行基因检测和产前诊断的普遍态度的资料很少。因此,本研究评估了遗传性听力损失的印度人进行此类测试的动机。二十八个有先天性听力障碍病史的家庭(23名听力障碍的父母有儿童/家庭成员为耳聋,4对夫妻双方都有耳聋,1名父母和孩子为耳聋)参加了一项半结构化调查,调查了他们的兴趣,态度,以及使用遗传和产前测试来进行耳聋的意图。与会者认为,耳聋个人的适当管理和护理受到有限的康复设施的束缚,这些设施具有重大的经济和社会负担。十九名(68%)选择了基因检测。二十六(93%)表示对产前诊断非常感兴趣,而19(73%)表示考虑终止受影响的胎儿。三对听觉伴侣选择了产前诊断,其中识别出了致病突变。在测试中,所有三个胎儿均受到影响,听证父母选择终止妊娠。这项研究提供了对印度听力障碍的不同观念及其对基因检测和产前诊断的影响的见解。

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