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儿童X连锁突发性疾病DFNX2,一种罕见的内耳发育异常,伴有混合性听力和前庭功能丧失。

X-Linked Gusher Disease DFNX2 in Children, a Rare Inner Ear Dysplasia with Mixed Hearing and Vestibular Loss.

作者信息

Dasgupta Soumit, Hong James, Morris Rhyanna, Iqbal Javed, Lennox-Bowley Amy, Saniasiaya Jeyasakthy

机构信息

Alder Hey Children's Hospital NHS Foundation Trust, Eaton Road, Liverpool L14 5AB, UK.

Faculty of Health and Medical Sciences, University of Liverpool, Liverpool L69 3BX, UK.

出版信息

Audiol Res. 2023 Aug 4;13(4):600-614. doi: 10.3390/audiolres13040052.

Abstract

Conductive hearing losses are typically present in disorders of the external/middle ear. However, there is a rare group of inner ear conditions called third windows that can also generate a conductive hearing loss. This is due to an abnormal connection between the middle and the inner ear or between the inner ear and the cranial cavity. X-linked gusher disorder is an extremely rare congenital inner ear dysplastic syndrome with an abnormal connection due to a characteristic incomplete cochlear partition type III and an incomplete internal auditory meatus fundus. The disorder is inherited in an X-linked fashion due to the mutation of the gene. We present two siblings diagnosed with the condition and their long-term follow-ups. They both presented audiovestibular symptoms and showed progressive mixed losses and bilateral vestibular weakness. They were treated with cochlear implant, digital amplification and with vestibular rehabilitation. Significant others around them were involved in their journey with the medical team, and in both, a very favourable outcome was achieved. This is the first time that we have reported evolving audiovestibular function with vestibular quantification in X-linked gusher disorder and emphasize on the multidisciplinary holistic approach to manage these children effectively.

摘要

传导性听力损失通常见于外耳/中耳疾病。然而,有一种罕见的内耳疾病称为第三窗病变,也可导致传导性听力损失。这是由于中耳与内耳之间或内耳与颅腔之间存在异常连接。X连锁性耳涌症是一种极其罕见的先天性内耳发育异常综合征,由于特征性的III型耳蜗分隔不完全和内耳道底不完全,导致连接异常。该疾病由于基因的突变而呈X连锁遗传方式。我们报告了两名被诊断为此病的兄弟姐妹及其长期随访情况。他们均出现了听前庭症状,表现为进行性混合性听力损失和双侧前庭功能减弱。他们接受了人工耳蜗植入、数字放大和前庭康复治疗。他们身边的重要他人参与了他们与医疗团队的治疗过程,两人均取得了非常良好的治疗效果。这是我们首次报告X连锁性耳涌症中通过前庭量化评估的听前庭功能演变情况,并强调采用多学科整体方法有效管理这些儿童。

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