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題 名 | Familial Congenital Ocular Motor Apraxia=家族性先天眼球運動失用症 |
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作 者 | 徐紅娜; 楊孟玲; 賴慧群; | 書刊名 | 長庚醫學 |
卷 期 | 25:6 2002.06[民91.06] |
頁 次 | 頁411-414 |
分類號 | 416.74 |
關鍵詞 | 先天性眼球運動失用症; 家族性; Congenital ocular motor apraxia; Familial; |
語 文 | 英文(English) |
中文摘要 | 先天性眼球運動失用症(congenital ocular motor apraxia)是一種少見的眼球運動障礙。其特徵為自主性水平運動啟動困難,但反射性水平運動則可能為正常。垂直性運動除了罕見病例報告外均為正常。病患之外觀特徵明顯-代償性頭部甩頭,以前庭眼球反射來達到眼球轉動之目的。罹病者常有閱讀困難及學習障礙。幸運的是,絕大多數病患隨著年齡增長有逐漸改善之趨勢。 自從西元1952年首例報告以來,陸續有零星病例被提出。其中除了少數為家族性外,均為散發性。本報告將提出四位病患,其中二位為兄弟,另外二位則為父女。對於其眼球運動檢查結果亦將有詳細描述。 |
英文摘要 | Congenital ocular motor apraxia (COMA) is a unique ocular motor disorder which is characterized by a deficit in initiation of voluntary horizontal eye movement with reserved feflex eye movement. Although a portion of cases with COMA were found to be associated with other abnormalities, COMA in most patients is an isolated disorder. The most characteristic appearance of these patients is compensatory head thrusts which usually become less evident with increasing age. Since Cogan firs described COMA in 1952, many cases have been reported. The majority of these occurred sporadically with only a few exceptions. We report on 4 patients with COMA. Two of them were siblings, and the other 2 patients were father and daughter. The ocular motility status is described in detail. |
本系統中英文摘要資訊取自各篇刊載內容。