Johnsen T, Larsen C, Friis J, Hougaard-Jensen F
ENT Department, Gentofte University Hospital, Hellerup.
J Laryngol Otol. 1987 Nov;101(11):1187-92. doi: 10.1017/s0022215100103470.
Seventeen unrelated Danish patients with Pendred's syndrome, whose case stories have not been published previously, are presented. Acoustic and vestibular functions were examined and endocrinological screening was performed. There was a great variation in hearing ability as well as in thyroid function. Furthermore, in contrast to previous investigations, normal caloric function was demonstrated in the majority. In all patients a Mondini malformation was demonstrated. On the basis of this investigation it is concluded that: (1) the Mondini defect is part of Pendred's syndrome; (2) the inherited Mondini malformation is the underlying cause of the sensorineural hearing impairment; and (3) the hearing sensitivity varies greatly in these patients.
本文报告了17例患有彭德莱德综合征的丹麦患者,他们之间没有亲缘关系,且其病例故事此前未曾发表。对他们进行了听觉和前庭功能检查,并进行了内分泌筛查。听力和甲状腺功能存在很大差异。此外,与之前的研究不同,大多数患者的冷热试验功能正常。所有患者均显示有Mondini畸形。基于这项研究得出以下结论:(1)Mondini缺陷是彭德莱德综合征的一部分;(2)遗传性Mondini畸形是感音神经性听力损失的根本原因;(3)这些患者的听力敏感度差异很大。