Ocular Manifestations in Patients with Sensorineural Hearing Loss.

IF 1.6 Q3 OPHTHALMOLOGY
Journal of Ophthalmic & Vision Research Pub Date : 2022-11-29 eCollection Date: 2022-10-01 DOI:10.18502/jovr.v17i4.12321
Haniah A Zaheer, Deepika C Parameswarappa, Myra A Zaheer, Jay Chhablani, Preeti Patil-Chhablani
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引用次数: 0

Abstract

Identification of ocular manifestations in patients with sensorineural hearing loss (SNHL) can have a large impact on the outcome and treatment of pediatric patients. Due to the common co-incidence of ocular manifestations and SNHL in children, both ophthalmologic and hearing loss screening and routine examinations must be conducted to minimize adverse outcomes and worsening of pathology. Early evaluation and diagnosis is imperative for intervention and further development of the patient. Co-incidence requires a thorough evaluation that includes a comprehensive history, examination, and diagnostic testing. In this article, a literature review was conducted to analyze the presentations of various diseases and syndromes, such as Alport Syndrome, Waardenburg Syndrome, Norrie Disease, Usher Disease, Stickler Syndrome, Marfan Syndrome, Congenital Rubella, and Hereditary Optic Neuropathies. We divided the various ocular pathologies into anterior and posterior segment presentations and associated systemic findings for better understanding. Additionally, this review aims to include an update on the management of patients with both ocular and hearing loss manifestations.

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感音神经性听力损失患者的眼部表现。
识别感音神经性听力损失(SNHL)患者的眼部表现对儿童患者的治疗效果和治疗方法有很大影响。由于儿童眼部表现和感音神经性听力损失(SNHL)的常见并发症,因此必须同时进行眼科和听力损失筛查和常规检查,以尽量减少不良后果和病理恶化。早期评估和诊断对于患者的干预和进一步发展至关重要。合并症需要进行全面的评估,包括综合病史、检查和诊断测试。本文通过文献综述分析了各种疾病和综合征的表现,如阿尔波特综合征、瓦登堡综合征、诺里病、乌舍尔病、斯蒂克勒综合征、马凡综合征、先天性风疹和遗传性视神经病变。为了更好地理解,我们将各种眼部病变分为前段和后段表现以及相关的系统性发现。此外,本综述还旨在介绍眼部和听力损失患者的最新治疗方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
3.60
自引率
0.00%
发文量
63
审稿时长
30 weeks
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