Evaluation and management of syndromic congenital hearing loss

被引：12
|
作者：
Casazza, Geoffrey [1 ,2 ]
Meier, Jeremy D. [1 ,2 ]
机构：
[1] Univ Utah, Sch Med, Div Otolaryngol, Salt Lake City, UT USA
[2] Primary Childrens Med Ctr, 100 North Mario Capecchi Dr,Suite 1300, Salt Lake City, UT 84113 USA
来源：
CURRENT OPINION IN OTOLARYNGOLOGY & HEAD AND NECK SURGERY | 2017年 / 25卷 / 05期
基金：
美国医疗保健研究与质量局;
关键词：
Pendred syndrome; syndromic hearing loss; Waardenburg syndrome; ENLARGED VESTIBULAR AQUEDUCT; TREACHER-COLLINS-SYNDROME; COCHLEAR IMPLANTATION; USHER-SYNDROME; LANGUAGE-DEVELOPMENT; CLINICAL-EVALUATION; PENDRED SYNDROME; TEMPORAL BONE; MOUSE MODEL; CHILDREN;
D O I：
10.1097/MOO.0000000000000397
中图分类号：
R76 [耳鼻咽喉科学];
学科分类号：
100213 ;
摘要：
Purpose of review The purpose of this review is to review the evaluation and management of children with syndromic hearing loss. Specific syndromes and the impact of those syndromes on managing hearing loss will be discussed. Recent findings Improved molecular testing has increased the ability to identify syndromes-associated hearing loss. Accurate diagnosis of syndromic hearing loss can guide discussions regarding prognosis and appropriate management options for the hearing impairment. Summary A significant portion of childhood hearing loss is associated with a syndrome. Depending on the syndrome, surgical intervention including a bone-anchored hearing aid or cochlear implant may be helpful. In the future, targeted gene therapies may become a viable option for treating syndromic hearing loss.
引用
收藏
页码：378 / 384
页数：7
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