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題 名 | 青年型糖尿病合併視神經萎縮--沃夫然症候群之病例報告=Juvenile Onset Diabetes Mellitus and Optic Atrophy-- A Case Report of Wolfram Syndrome |
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作 者 | 陳俊寰; 陳宏任; 翁林仲; 周介仁; 謝瑞玟; 李燕晉; | 書刊名 | 中華民國眼科醫學會雜誌 |
卷 期 | 37:3 1998.09[民87.09] |
頁 次 | 頁297-303 |
分類號 | 415.6687 |
關鍵詞 | 沃夫然症候群; 青年型糖尿病; 視神經萎縮; Wolfram syndrome; Insulin dependent diabetes mellitus; IDDM; Primary optic atrophy; High frequency hearing loss; |
語 文 | 中文(Chinese) |
中文摘要 | 沃夫然症候群Wolfram (DIDMOAD) Syndrome,是指合併有青年型糖尿病,視神 經萎縮,耳聾,以及尿崩症等症狀。通常糖尿病是第一個表徵,接著出現原發性視神經萎縮, 然後感音性聽力受損,最後可能伴隨尿崩症。本篇報告一位19歲男孩,自9歲發生青年型 糖尿病,從11歲開始出現視力減退並伴隨聽力喪失。經檢查發現有原發性視神經萎縮,中 等度高頻聽力喪失,以及多尿的現象。本篇將以12年的追蹤,報告其臨床變化、眼底、視 野及眼神經學方面的表現。 |
英文摘要 | Wolfram (DIDMOAD) Syndrome was originally described as a combination of juvenile onset diabetes mellitus, optic atrophy, deafness, and diabetes insipidus beginning in childhood. Diabetes mellitus usually occurs as the first manifestation of this syndrome, followed by the development of primary optic atrophy, neurosensory hearing loss, and finally diabetes insipidus which although not always occurs. We report a 19-year-old boy developed diabetes mellitus at age of 9. He complained of decreased vision and then hearing loss for eight years. Primary optic atrophy, moderate hearing loss at high frequency, and polyuria were found in later years. The clinical course, and neuroophthalmological characteristics were described in our follow-up for 12 years. |
本系統中英文摘要資訊取自各篇刊載內容。