一名戈登哈尔综合征患儿的耳朵畸形及其听力治疗。

Andrés González Fernández, Manuela Del Carmen Zapata, José Zubicaray Ugarteche
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引用次数: 0

摘要

Goldenhar综合征是一种罕见的先天性疾病,其特征是源自第一和第二鳃弓的结构发育缺陷。此病包括一系列症状,包括颅面、眼、椎体和耳部异常。我们提出的情况下,6岁的女孩右颞骨发育不全和耳前标签从出生,导致诊断为戈登哈综合征。她表现出各种中耳和外耳缺陷,她的听力学治疗对于确保最佳的神经和语言发育至关重要。在青春期,如果耳咽管保持稳定,可以考虑手术修复听骨链。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Ear malformation in a child with Goldenhar syndrome and its appropriate audiological management.

Goldenhar syndrome is a rare congenital disorder characterized by defects in the development of structures derived from the first and the second branchial arches. This condition encompasses a range of symptoms, including craniofacial, ocular, vertebral, and auricular abnormalities. We present the case of a 6-year-old girl with right temporal bone hypoplasia and preauricular tag from birth, leading to a diagnosis of Goldenhar syndrome. She exhibited various middle and external ear defects, and her audiological treatment was crucial in ensuring optimal neurological and speech development. In adolescence, if the Eustachian tube remains stable, surgical repair of the ossicular chain may be considered.

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