Pinelli V, Masi R, Partipilo P, Pierro V, Tieri L
E.N.T. Department, Bambino Gesù Hospital, Rome, Italy.
Basic Life Sci. 1988;48:149-52. doi: 10.1007/978-1-4684-8712-1_20.
The AA report a clinical and radiological study performed in 18 achondroplastic patients in order to achieve a nosological settlement of the otological impairments. They found two main otological syndromes; one, a congenital dysplasic syndrome, showing permanent conductive or sensory-neural hearing loss due to malformations of the middle ear or of the inner ear; the other, an inflammatory tubal tympanic syndrome with transient conductive hearing loss, which is relatively frequent in achondroplastic patients, but seems not related to the main disease.
AA报道了一项针对18名软骨发育不全患者进行的临床和放射学研究，目的是对耳部损伤进行疾病分类。他们发现了两种主要的耳部综合征；一种是先天性发育异常综合征，由于中耳或内耳畸形导致永久性传导性或感音神经性听力损失；另一种是炎症性咽鼓管鼓室综合征，伴有短暂性传导性听力损失，在软骨发育不全患者中相对常见，但似乎与主要疾病无关。
