先天性甲状腺功能减退症患者感音神经性听力损失的完全恢复。

IF 1 4区 医学 Q3 AUDIOLOGY & SPEECH-LANGUAGE PATHOLOGY
Jacline G Phillips, Samantha Fabian, Erin W Adkins, Eleanor P Kiell
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引用次数: 0

摘要

先天性甲状腺功能减退症(CH)是世界上最容易预防的智力残疾原因之一。筛查项目导致早期发现CH,与基线相比,补充足够甲状腺的儿童在整体神经心理测试中有轻微的长期差异。然而,即使早期补充足够的甲状腺激素,高达四分之一的先天性先天性甲状腺疾病患儿仍有听力损失。我们报告一例罕见的先天性甲状腺功能减退患者,在早期甲状腺激素替代后听力完全恢复。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Full Recovery of Sensorineural Hearing Loss in a Patient with Congenital Hypothyroidism.

Congenital hypothyroidism (CH) is one of the most preventable causes of intellectual disability in the world. Screening programs have led to earlier detection of CH, and children with adequate thyroid supplementation can have minor long-term differences in overall neuropsychological testing compared to baseline. However up to one- fourth of children born with CH suffer from hearing loss even with early and adequate thyroid hormone supplementation. We report a rare case of a patient with hearing loss attributed to congenital hypothyroidism who had complete recovery of hearing after early thyroid hormone replacement.

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来源期刊
CiteScore
3.10
自引率
0.00%
发文量
46
审稿时长
6-12 weeks
期刊介绍: The Journal of the American Academy of Audiology (JAAA) is the Academy''s scholarly peer-reviewed publication, issued 10 times per year and available to Academy members as a benefit of membership. The JAAA publishes articles and clinical reports in all areas of audiology, including audiological assessment, amplification, aural habilitation and rehabilitation, auditory electrophysiology, vestibular assessment, and hearing science.
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