Stapes surgery in osteogenesis imperfecta -: A clinical study of 16 patients

被引:2
|
作者
Hultcrantz, Malou [1 ]
Saaf, Maria [1 ]
机构
[1] Karolinska Univ Hosp, Dept Otorhinolaryngol, SE-17176 Stockholm, Sweden
来源
关键词
D O I
10.1159/000098826
中图分类号
R76 [耳鼻咽喉科学];
学科分类号
100213 ;
摘要
Osteogenesis Imperfecta (01), is a genetic disease of connective tissue, with the main feature of bone fractures, accompanied by blue sclerae and hearing loss. Hearing loss affects about 50% of the patients, beginning in the second and third decade of life. The hearing loss is progressive, starting with a conductive loss, then a mixed and later on a sensorineural loss. There are similarities between otosclerosis, although 01 is a distinct entity. The diseases are treated in the same surgical way. The result is, however, not as good in 01 as in otosclerosis according to different reports. A screening study of 15 patients with 01 at the Karolinska Hospital, Sweden, has been performed, differing in age from 25-60. Audiometric examinations have been measured of both air and bone conduction. About 50% of the included patients had hearing loss. Three of the patients wore hearing aids. Of these 15 patients, only 4 had been operated on with stapes surgery. One of these patients needs a new operation. An indication for stapes surgery was found in about 50% of the investigated 01 patients. Copyright (c) 2007 S. Karger AG, Basel
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页码:222 / 225
页数:4
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