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一名13三体综合征患者的异位睫状上皮分化

Heterotopic ciliary epithelial differentiation in a patient with trisomy 13.

作者信息

Michon J J, Borges J M, Tso M O

机构信息

Georgiana Dvorak Theobald Ophthalmic Pathology Laboratory, Department of Ophthalmology, University of Illinois, College of Medicine, Chicago 60612.

出版信息

J Pediatr Ophthalmol Strabismus. 1991 Jan-Feb;28(1):23-7.

PMID:2019954
Abstract

A premature infant was born with congenital anomalies suggestive of trisomy 13, confirmed by karyotype analysis. Pathologic examination of the eyes revealed typical features of trisomy 13, including microphthalmos, extensive colobomata, and retinal dysplasia. A heterotopic ciliary body had also developed in the posterior segment of the left eye in the region of the posterior coloboma. The development of a well-formed ciliary body in the posterior segment of the eye questions the hypothesis that physical contact between the lens primordium and neuroepithelium is required for ciliary body development.

摘要

一名早产婴儿出生时伴有提示13三体综合征的先天性异常,经核型分析确诊。眼部病理检查显示13三体综合征的典型特征,包括小眼畸形、广泛的脉络膜缺损和视网膜发育异常。在左眼后段后脉络膜缺损区域还出现了异位睫状体。在眼后段出现发育良好的睫状体,对晶状体原基与神经上皮之间的物理接触是睫状体发育所必需的这一假说提出了质疑。

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