Santos Regie Lyn P, Häfner Franziska M, Huygen Patrick L M, Linder Thomas E, Schinzel Albert A, Spillmann Thomas, Leal Suzanne M
Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Tex. 77030, USA.
Audiol Neurootol. 2006;11(5):269-75. doi: 10.1159/000093525. Epub 2006 May 23.
This article describes the hearing impairment (HI) phenotype which segregates in a large multi-generation Swiss-German family with autosomal dominant nonsyndromic HI. The locus segregating within this pedigree is located on chromosome 4q35-qter and is designated as DFNA24. For this pedigree, audiometric data on 25 hearing-impaired family members are available. It was demonstrated that within this kindred the HI is sensorineural, bilateral, prelingual in onset, and progressive throughout life. Age-related typical audiograms depict steeply down-sloping curves, with moderate high-frequency HI at birth, then steady progression to moderate HI in the low frequencies, severe HI at mid-frequencies and profound HI at high frequencies by age 70. Annual threshold deterioration was approximately 0.5 dB/year at 1-2 kHz after correction for presbycusis.
本文描述了一种听力障碍(HI)表型,它在一个大型的多代瑞士德裔家族中分离,该家族患有常染色体显性非综合征性HI。在这个家系中分离的基因座位于4号染色体q35 - qter上,被命名为DFNA24。对于这个家系,有25名听力受损家庭成员的听力测定数据。结果表明,在这个家族中,HI是感觉神经性的、双侧的、发病于语言前阶段,且终生进展。与年龄相关的典型听力图呈现出陡峭的下坡曲线,出生时为中度高频HI,然后稳步发展为低频中度HI、中频重度HI以及70岁时高频极重度HI。在校正老年性耳聋后,1 - 2千赫兹处的年阈值恶化约为0.5分贝/年。