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Wagner综合征又名遗传性玻璃体视网膜变性,于1938年首次报道。表现为玻璃体脱水浓缩、膜状物形成、混浊,脉络膜和视网膜色素性改变,视网膜血管变细,有白鞘,血管周围脉络膜硬化和色素团块,视网膜格子样变性,周边视野缩小,近视,白内障等。 Wagner综合征具有难以治疗的并发症,包括视网膜脱离和新生血管性青光眼。本文介绍1例(女性,44岁)Wagner综合征合并视网膜脱离和虹膜新生血管病变的患者。作者首先给予视网膜复位手术治疗,术后发现虹膜与
Wagner syndrome, also known as hereditary vitreoretinal degeneration, was first reported in 1938. The performance of the vitreous dehydration and condensation, the formation of membranous, turbid, choroidal and retinal pigmented changes, thinning of the blood vessels of the retina, a white sheath, perivascular choroidal sclerosis and pigment mass, retinal lattice degeneration, peripheral vision reduction, myopia, cataract . Wagner syndrome has refractory complications, including retinal detachment and neovascular glaucoma. This article describes one patient (female, 44 years old) with Wagner’s syndrome complicated with retinal detachment and iris neovascular disease. The authors first give retinal reattachment surgery, after surgery found iris and