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[艾卡迪综合征:一例病例报告]

[Aicardi syndrome: a case report].

作者信息

Lin C K, Tsai R K, Jong Y J

机构信息

Department of Ophthalmology, Kaohsiung Medical College, Taiwan, Republic of China.

出版信息

Gaoxiong Yi Xue Ke Xue Za Zhi. 1992 Dec;8(12):692-6.

PMID:1296050
Abstract

A 5-year-old girl had suffered from infantile spasms since 3 months of age. Cranial computerized tomography revealed agenesis of the corpus callosum. Abnormal ocular fundus features consisted of bilateral disc colobomas and lacunar pigment change in her right eye. The clinical presentations were consistent with Aicardi syndrome. The ophthalmologic manifestations of Aicardi syndrome will be discussed in this paper.

摘要

一名5岁女孩自3个月大起就患有婴儿痉挛症。头颅计算机断层扫描显示胼胝体发育不全。眼部异常特征包括双侧视盘缺损和右眼的片状色素改变。临床表现符合艾卡迪综合征。本文将讨论艾卡迪综合征的眼科表现。

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