Chorioretinal coloboma: clinical presentation complications and treatment alternatives

A. Altıntaş
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引用次数: 1

Abstract

Choroio Retinal coloboma (CRC) characterized by congenital absence of part of the retinal pigment epithelium and choroid, caused by the defective closure of the embryonic fissure, which normally develops gradually between sixth and seventh weeks of fetal life. Colobomas present various parts of ocular tissue such as iris and /or uvea, lens, optic nerve or eyelid. Since it is embriological pathology CRC may also be associated with other ocular pathologies such as cataract, microphthalmia, anophthalmia.1−4
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绒毛膜视网膜缺损:临床表现、并发症及治疗选择
Choroio Retinal coloboma (CRC)以先天性视网膜色素上皮和脉络膜部分缺失为特征,由胚胎裂隙闭合缺陷引起,通常在胎儿生命的第6 - 7周之间逐渐发展。结肠瘤出现在眼部组织的各个部位,如虹膜和/或葡萄膜、晶状体、视神经或眼睑。由于CRC是一种胚胎病理学,它也可能与其他眼部病变相关,如白内障、小眼症、无眼症等
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