首页> 外文期刊>Journal of computer assisted tomography >Computed tomographic findings of X-Linked deafness: A spectrum from child to mother, from young to old, from boy to girl, from mixed to sudden hearing loss
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Computed tomographic findings of X-Linked deafness: A spectrum from child to mother, from young to old, from boy to girl, from mixed to sudden hearing loss

机译:X线性耳聋的计算机断层扫描结果:从儿童到母亲,从年轻到老年,从男孩到女孩,从混合到突然的听力丧失的频谱

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PURPOSE: Congenital mixed hearing loss associated with fixed stapes footplate is a rare disorder transmitted through X-linked inheritance. The purpose of this study was to report the radiologic findings of X-linked deafness with middle ear anomalies in affected children and young patients and in carrier women. MATERIALS AND METHODS: The computed tomographic and audiometric findings of 7 subjects (4 affected children and young patients, 1 of whom is a girl; 2 carrier mothers; and a man who presented with sudden hearing loss) from different families were analyzed. RESULTS: Computed tomography showed bulbous dilatation of the fundi of the internal auditory canals, incomplete bony separation between the basal turn of the cochleas and the lateral ends of the internal auditory canal, deficiency of the modiolus, enlarged first part of the facial nerve, and dilatation of the superior and the inferior vestibular nerve canal and the singular canal. Besides these characteristic findings, dilatation of the vestibular aqueduct was seen except in the man. Middle ear anomalies including oval and/or round window and/or stapes abnormalities were also detected in three affected patients. The carrier mothers had milder forms of some characteristic findings. CONCLUSIONS: Because of the risks of stapes surgery in X-linked deafness, recognition of the characteristic imaging features of these disorders is important. Especially in young patients with mixed hearing loss, temporal bone computed tomography should be performed before stapes surgery to avoid the complication of stapes gusher. Middle ear anomalies might be highly associated with X-linked deafness.
机译:目的:先天性混合性聋与固定骨足板相关,是一种罕见的疾病,通过X连锁遗传传播。这项研究的目的是报告在患病的儿童和年轻患者以及携带者妇女中,X线性耳聋与中耳异常的放射学表现。材料与方法:分析了来自不同家庭的7位受试者(4位受影响的儿童和年轻患者,其中1位是女孩; 2位带载体的母亲;以及一名突然失聪的男人)的计算机断层扫描和听力检查结果。结果:计算机体层摄影术显示内耳道的球根扩张,耳蜗基底转弯与内耳道的侧端之间的骨分离不完全,耳蜗缺损,面部神经的第一部分扩大以及前庭和下庭神经管和奇管扩张。除了这些特征性发现外,除男性外,还观察到前庭导水管的扩张。在三名受影响的患者中也检测到了中耳异常,包括椭圆形和/或圆形窗口和/或sta骨异常。承运人的母亲有较温和的形式,有一些特征性发现。结论:由于X型耳聋有骨手术的风险,因此认识这些疾病的特征性影像学特征非常重要。尤其是在患有混合性听力损失的年轻患者中,骨手术前应进行颞骨计算机体层摄影术,以避免of骨涌出的并发症。中耳异常可能与X连锁性耳聋高度相关。

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