Congenital anterior segment epithelialisation (case).

Australian journal of ophthalmology Pub Date : 1983-08-01
L W Hirst
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引用次数: 0

Abstract

Posterior polymorphous endothelial dystrophy and iridocorneal endothelial syndrome share common specular microscopic findings, clinical course, and some histopathological features. Despite differences in inherited trait and severity of disease a common pathogenetic mechanism for the two diseases is suggested. This consists of congenital epithelialisation of the posterior corneal surface during embryogenesis with migration of these cells around the anterior segment uninhibited by surrounding normal endothelium.

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先天性前段上皮化(1例)。
后多形性内皮营养不良和虹膜角膜内皮综合征具有共同的镜下显微镜表现、临床过程和一些组织病理学特征。尽管遗传性状和疾病严重程度不同,但两种疾病的共同发病机制被提出。这包括胚胎发生时角膜后表面的先天性上皮化,这些细胞不受周围正常内皮的抑制,在前段周围迁移。
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