牵牛花综合征(Moroing Glory Syndrome)系一种罕见的先天性视盘异常,Kindler(1970)首次报道。目前已知此综合征常伴发后极部视网膜脱离,但病因尚不明确。本文报道一例双侧性牵牛花综合征,高度近视并发左眼裂孔性视网膜脱离。本文回顾有关文献,探讨此综合征的病因及其视网膜脱离的治疗。患者女性14岁,诉左眼视力模糊10天,伴有多发性中心和颞侧闪光感。既往史有双侧视乳头缺损性病变及视觉性眼震。病史记录示右眼戴-12D接触镜,左眼戴-16D接触镜,最佳矫正视力分别为0.05和0.1。初诊时患者右眼最佳矫正 Moroing Glory Syndrome is a rare congenital optic disc abnormality, first reported by Kindler (1970). It is now known that this syndrome often accompanied by posterior pole retinal detachment, but the etiology is not yet clear. This article reports a case of bilateral morning glory syndrome, high myopia with left-sided retinal detachment. This article reviews the literature to explore the etiology of this syndrome and its treatment of retinal detachment. A 14-year-old woman complained of blurred vision in the left eye for 10 days, with multiple centers and temporal flares. Past history of bilateral optic disc defect lesions and visual nystagmus. History records show that the right eye wear -12D contact lens, left eye wearing -16D contact lens, the best corrected visual acuity were 0.05 and 0.1. The patient’s right eye best corrected at first visit