Hearing impairment in 18q deletion syndrome

被引：0
|
作者：
Jayarajan, V
Swan, IRC
Patton, MA
机构：
[1] Royal Surrey Cty Hosp, Dept Audiol Med, Guildford GU2 7XX, Surrey, England
[2] Glasgow Royal Infirm, Dept Otolaryngol, Glasgow G4 0SF, Lanark, Scotland
[3] Univ London St Georges Hosp, Sch Med, SW Thames Reg Genet Serv, London SW17 0RE, England
来源：
JOURNAL OF LARYNGOLOGY AND OTOLOGY | 2000年 / 114卷 / 12期
关键词：
deafness; chromosome; human; pair; 18; chromosome deletion; ear canal;
D O I：
暂无
中图分类号：
R76 [耳鼻咽喉科学];
学科分类号：
100213 ;
摘要：
The 18q- syndrome is associated with hearing impairment in 50-80 per cent of cases. The hearing loss may be sensorineural or conductive. A high proportion of cases are associated with narrow or stenosed external auditory canals. This may be a useful clinical pointer to the syndrome. Two cases with impaired hearing are presented in this paper including one case with complex external ear and middle ear malformations. The clinical and audiological features in each case are described.
引用
收藏
页码：963 / 966
页数：4
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