Parker M J, Fortnum H M, Young I D, Davis A C, Mueller R F
MRC Institute of Hearing Research, University Park, Nottingham, United Kingdom.
Audiology. 2000 Jul-Aug;39(4):226-31. doi: 10.3109/00206090009073083.
The objective of the study was to investigate childhood hearing impairment in a population-based sample from a genetic perspective. Participants included 82 families with hearing-impaired children (aged 4-13) previously ascertained in the Trent Health Region. A questionnaire was mailed to all families, followed by a home visit and Connexin-26 35delG mutation screen. The Connexin-26 35delG mutation was identified in seven families (approximately 10 per cent of non-syndromal hearing impairment). Children of these families were significantly more likely than children with other modes of inheritance to have a profound hearing loss with a flat audiogram profile. The families of children with a significant admission to a neonatal intensive care unit were significantly less likely to have had genetic counselling. Eight families visited were found to have features suggestive of a genetic syndrome that had not been previously assigned a specific diagnosis. The study concluded that hearing-impaired children should be investigated systematically according to an agreed-upon protocol, which should include Connexin-26 35delG mutation analysis at least for those with severe-to-profound hearing loss.
该研究的目的是从遗传学角度对一个基于人群的样本中的儿童听力障碍进行调查。参与者包括82个有听力受损儿童(年龄在4至13岁)的家庭,这些家庭先前已在特伦特健康地区被确定。向所有家庭邮寄了一份问卷,随后进行了家访和连接蛋白-26 35delG突变筛查。在7个家庭中发现了连接蛋白-26 35delG突变(约占非综合征性听力障碍的10%)。与其他遗传方式的儿童相比,这些家庭的儿童更有可能出现重度听力损失且听力图呈平坦型。有儿童因重症入住新生儿重症监护病房的家庭接受遗传咨询的可能性显著更低。在走访的8个家庭中,发现有一些特征提示存在尚未得到明确诊断的遗传综合征。该研究得出结论,应根据商定的方案对听力受损儿童进行系统调查,该方案至少应对那些重度至极重度听力损失的儿童进行连接蛋白-26 35delG突变分析。