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題 名 | 先天性纖維化症候群--病例報告 |
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作 者 | 莊雪霞; 詹秋忠; 林永鋒; 徐富民; | 書刊名 | 中華民國眼科醫學會雜誌 |
卷 期 | 31:3 1992.09[民81.09] |
頁 次 | 頁123-126 |
分類號 | 416.755 |
關鍵詞 | 先天性纖維化症候群; 眼外肌; 遺傳疾病; Congenital ocular fibrosis syndrome; Congenital ptosis; Hypotropia; |
語 文 | 中文(Chinese) |
中文摘要 | 先天性纖維化症候群是一少見的家族性遺傳疾病。本篇報告一名18歲男 性病患,自幼皆為下巴朝上,眼瞼下垂,雙眼為內斜及下斜眼位,無法做任何水 平或垂直方向之眼球轉動,但上視時,有內聚運動;本篇特提出一病例,敘述其 臨床特徵,追蹤其家族罹患情形,並討論其手術治療方法。 |
英文摘要 | Congenital fibrosis syndrome is a rare familial hereditary disease, characterized by fibrotic change of extraocular muscles. Herein we present a typical case with chin up, both eyes are fixed in down and inward gaze, lack of levator function, convergence during intended up gaze. This 18 year-old young man has a positive family history, traced for three generations. Surgical treatment had improved the eye alignment and chin up posture. For lack of Bell's phenomonen, undercorrection of the ptosis is necessary to avoid exposure keratititis. |
本系統中英文摘要資訊取自各篇刊載內容。