Cohen M, Francis M, Coffey R, Pembrey M E, Luxon L M
Academic Division of Audiological Medicine, Institute of Laryngology and Otology, UCL Medical School, London, UK.
Acta Otolaryngol. 1997 May;117(3):337-42. doi: 10.3109/00016489709113404.
Pure-tone audiograms and acoustic reflex thresholds were obtained in 24 presumed obligate carriers of autosomal recessive non-syndromic hearing loss and 30 sex and age appropriate control subjects, with a view to evaluating the prevalence of abnormalities on these tests in the two groups, and a possible link between the findings on the two tests, which may help to localize threshold deficits and/or abnormal configurations to different sections of the reflex arc. Six (25%) of the carriers and one control subject had abnormal audiograms, inferred to be of genetic aetiology through careful exclusion of environmental risk factors. Four additional carriers had acoustic reflex threshold abnormalities. None of the carriers had an abnormality on both tests. The audiometric configurations and acoustic reflex patterns of abnormality were diverse, and may be a reflection of the genetic heterogeneity in ARNSHL.
对24名推定的常染色体隐性非综合征性听力损失纯合子携带者和30名性别与年龄匹配的对照受试者进行了纯音听力图和听觉反射阈值测试,旨在评估两组中这些测试异常的发生率,以及两项测试结果之间可能存在的联系,这可能有助于将阈值缺陷和/或异常构型定位到反射弧的不同部位。6名(25%)携带者和1名对照受试者的听力图异常,通过仔细排除环境风险因素推断为遗传病因。另有4名携带者存在听觉反射阈值异常。没有携带者两项测试均异常。听力测定异常构型和听觉反射异常模式各不相同,可能反映了常染色体隐性非综合征性听力损失的遗传异质性。