Simultaneous bilateral cochlear implantation in a case of waardenburg syndrome – A case report and review of literature

KN Arif, J. Passey, M. Ali, Taorem Medhabati Devi
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Abstract

We report a case of Waardenburg Syndrome (WS) who underwent simultaneous bilateral cochlear implantation and the evolution of auditory performance over a 5 year follow-up. Examination revealed a white forelock with iris heterochromia and confluent eyebrows (synophoris). Audiometric evaluation revealed bilateral profound sensorineural hearing loss. High resolution tomography of temporal bone showed normal inner ear anatomy and subsequently child underwent bilateral cochlear implantation which was followed by regular postoperative rehabilitation and speech therapy.
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同时双侧人工耳蜗植入waardenburg综合征1例报告并文献复习
我们报告一例Waardenburg综合征(WS)患者同时接受双侧人工耳蜗植入,并在5年的随访中听力表现的演变。检查发现白额发,虹膜异色,眉毛汇合。听力评估显示双侧深度感音神经性听力损失。颞骨高分辨率断层扫描显示内耳解剖正常,随后患儿接受双侧人工耳蜗植入,术后常规康复和言语治疗。
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