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晶状体和瞳孔异位伴皮肤、毛发及睫毛斑片状色素脱失:一种新的关联。

Ectopia lentis et pupillae with patchy depigmentation of the skin, hair and lashes: a new association.

作者信息

Manitto M P, Brancato R, Lombardo N, Zarrella M, Nucci P

机构信息

Department of Ophthalmology and Visual Sciences, Scientific Institute San Raffaele Hospital, University of Milano, Italy.

出版信息

Eur J Ophthalmol. 1998 Jul-Sep;8(3):188-90. doi: 10.1177/112067219800800313.

Abstract

We describe a case of a four year-old boy, with congenital ectopia lentis et pupillae, who developed patchy unilateral depigmentation of the skin, hair and lashes. The association between ectopia lentis et pupillae and transillumination of the iris is well documented in the literature, but it has never been reported with skin hypopigmentation.

摘要

我们描述了一例患有先天性晶状体和瞳孔异位的4岁男孩,他出现了单侧皮肤、毛发和睫毛的斑片状色素脱失。晶状体和瞳孔异位与虹膜透照之间的关联在文献中有充分记载,但皮肤色素减退的情况从未有过报道。

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