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特雷彻·柯林斯综合征的眼部表现。

Ocular findings in Treacher Collins syndrome.

作者信息

Wang F M, Millman A L, Sidoti P A, Goldberg R B

机构信息

Department of Ophthalmology, Montefiore Medical Center, Albert Einstein College of Medicine, Bronx, New York.

出版信息

Am J Ophthalmol. 1990 Sep 15;110(3):280-6. doi: 10.1016/s0002-9394(14)76345-7.

Abstract

We examined 14 patients from nine families referred with the diagnosis of Treacher Collins syndrome. We noted seven significant ocular findings including the following: a subnormal horizontal palpebral fissure length and inferomedial displacement of the lateral canthus in primary gaze; further medial displacement (4.0 mm or more) of the lateral canthus with resultant shortening of the horizontal fissure length on forced eyelid closure (fissure narrowing sign); partial-thickness eyelid colobomata localized to the nasal one half to two thirds of the lower eyelids; bilateral absence of the inferior lacrimal puncta; bilateral blepharoptosis; inferior displacement of the palpebral fissures; and regular astigmatism without any consistent orientation of the axis of astigmatism relative to the lower eyelid defects, blepharoptosis, or lateral canthus. The fissure narrowing sign correlates with known anatomic deficiencies in the Treacher Collins syndrome and may prove valuable in confirming the diagnosis in patients who lack certain typical features.

摘要

我们检查了来自9个家庭的14例被诊断为特雷彻·柯林斯综合征的患者。我们发现了7项显著的眼部表现,包括以下内容:在第一眼位时,水平睑裂长度低于正常且外眦向内下移位;用力闭眼时外眦进一步向内移位(4.0毫米或更多),导致水平睑裂长度缩短(睑裂狭窄征);下睑鼻侧一半至三分之二处有部分厚度的睑裂缺损;双侧下泪点缺失;双侧上睑下垂;睑裂向下移位;以及规则散光,散光轴相对于下睑缺损、上睑下垂或外眦无任何一致的方向。睑裂狭窄征与特雷彻·柯林斯综合征中已知的解剖学缺陷相关,对于缺乏某些典型特征的患者,可能在确诊中具有重要价值。

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