摘要
先天性纤维化综合征临床表现复杂 ,病因不明 ,是眼外肌病中诊断及治疗的难点。目前已发现先天性纤维化综合征有 5个遗传位点、1个致病基因。更深入的分子遗传学研究结果是对先天性纤维化综合征进行恰当诊断、分类及治疗的重要依据。本文对先天性眼外肌纤维化基因定位。
出处
《国际眼科纵览》
2004年第1期61-63,共3页
International Review of Ophthalmology
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