原田氏病被认为是黑色素细胞的自身免疫性疾病。除可引起葡萄膜炎、脑膜炎、眩晕、脱发外,还可引起内耳功能障碍。作者研究了过去12年间所治疗的有听力障碍的34名63耳原日氏病患者,并与突发性耳聋做以比较,得出以下结论:①听力障碍多为轻度两侧性内耳功能障碍性耳聋。初诊时听力水平在31.2±11.8dB。54%为高频部障碍型,25.4%呈水平型,20.6%为山型。42.9%的人缺乏自觉性听力障 Harada’s disease is considered an autoimmune disease of melanocytes. In addition to causing uveitis, meningitis, dizziness, hair loss, but also can cause inner ear dysfunction. The authors studied 34 hearing-impaired patients with 63-year-old forms of JJD who were treated in the past 12 years and compared them with sudden deafness. The following conclusions were reached: ① Hearing impairment was mostly mild bilateral dysfunction of the inner ear Sexual deafness. Hearing level at the first visit was 31.2 ± 11.8 dB. 54% were high-frequency obstruction type, 25.4% were horizontal type and 20.6% were mountain type. 42.9% of people lack conscious hearing loss