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一例与科茨综合征相关的色素性视网膜炎。

A case of retinitis pigmentosa associated with Coats' syndrome.

作者信息

Yuguchi M, Majima A

出版信息

Ophthalmic Paediatr Genet. 1984 Dec;4(3):177-82. doi: 10.3109/13816818409006118.

DOI:10.3109/13816818409006118
PMID:6545394
Abstract

The association of bilateral retinitis pigmentosa with Coats' syndrome is reported. Four lesions of vascular telangiectasis with yellowish exudates were treated by xenon photocoagulation or cryocautery. Seven months later, new vascular changes occurred in another quadrant of the fundus. Since xenon photocoagulation could not be performed because of the patient's aversion to pain, argon laser photocoagulation was used but found ineffective. Cryocautery was necessary to treat the exudation over one quadrant, though xenon photocoagulation was effective in small lesions.

摘要

报告了双侧视网膜色素变性与科茨综合征的关联。对4处伴有淡黄色渗出物的血管扩张性病变进行了氙光凝或冷冻治疗。7个月后,眼底另一象限出现了新的血管变化。由于患者对疼痛的厌恶而无法进行氙光凝,遂使用氩激光光凝,但发现无效。尽管氙光凝对小病变有效,但仍需要冷冻治疗一个象限的渗出物。

相似文献

1
A case of retinitis pigmentosa associated with Coats' syndrome.一例与科茨综合征相关的色素性视网膜炎。
Ophthalmic Paediatr Genet. 1984 Dec;4(3):177-82. doi: 10.3109/13816818409006118.
2
Autosomal dominant retinitis pigmentosa and Coats'-like disease.常染色体显性遗传性视网膜色素变性和类科茨病。
Int Ophthalmol. 1985 Sep;8(3):147-51. doi: 10.1007/BF00136491.
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[Familial occurrence of Coats' syndrome combined with retinopathia pigmentosa].[科茨综合征合并色素性视网膜炎的家族性发病情况]
Klin Monbl Augenheilkd. 1972 Feb;160(2):158-63.
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A novel RPGR exon ORF15 mutation in a family with X-linked retinitis pigmentosa and Coats'-like exudative vasculopathy.一个患有X连锁视网膜色素变性和类Coats渗出性血管病变的家族中发现一种新的RPGR外显子ORF15突变。
Am J Ophthalmol. 2006 Jan;141(1):208-10. doi: 10.1016/j.ajo.2005.07.077.
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Coats'-type retinitis pigmentosa.科茨氏型视网膜色素变性
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Ultra-widefield imaging in Coats'-type retinitis pigmentosa.科茨样视网膜色素变性中的超广角成像
Indian J Ophthalmol. 2018 Jul;66(7):997-998. doi: 10.4103/ijo.IJO_1109_17.
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Retinitis pigmentosa: clinical observations and correlations.视网膜色素变性:临床观察与相关性
Trans Am Ophthalmol Soc. 1983;81:693-735.
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[Association of retinitis pigmentosa and coats' syndrome. Review of the literature apropos of 2 new cases].
Bull Soc Ophtalmol Fr. 1981 Nov;81(11):1023-8.
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Autosomal recessive retinitis pigmentosa with preserved para-arteriolar retinal pigment epithelium.常染色体隐性遗传性视网膜色素变性伴视网膜动脉旁色素上皮保留。
Am J Ophthalmol. 1994 Oct 15;118(4):430-9. doi: 10.1016/s0002-9394(14)75792-7.
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Coats-type retinitis pigmentosa in a 4-year-old child.一名4岁儿童的科茨样视网膜色素变性。
Am J Ophthalmol. 1997 Dec;124(6):846-8. doi: 10.1016/s0002-9394(14)71707-6.

引用本文的文献

1
Exudative retinopathy in a girl with Alström syndrome due to a novel mutation.一名因新突变患有阿尔斯特伦综合征的女孩出现渗出性视网膜病变。
Br J Ophthalmol. 2007 Jul;91(7):983-4. doi: 10.1136/bjo.2005.088781.
2
Advanced Coats' disease.晚期外层渗出性视网膜病变
Trans Am Ophthalmol Soc. 1991;89:371-476.