Meire F M, Van Egmond J, Hanssens M
Department of Ophthalmology, University Hospital, Ghent.
Bull Soc Belge Ophtalmol. 1992;245:91-7.
Children with CMC present with blue sclerae, megalocornea, hypoplastic and translucent irides, miosis and high myopia. The lenses may be dislocated as in familial Marfan syndrome but they are often in place and microspherophakic. The clinical history of a boy with CMC is presented. Pathological examination of the eyes showed megalophthalmos with thinned sclera, anomalies of the chamber angle and iris, ill-developed ciliary body and choroid and a small in situ lens.
患有先天性中胚层发育不良性角膜营养不良(CMC)的儿童表现为巩膜发蓝、角膜巨大、虹膜发育不全且半透明、瞳孔缩小和高度近视。晶状体可能像家族性马方综合征那样脱位,但它们通常位置正常且呈小球形晶状体。本文介绍了一名患有CMC的男孩的临床病史。眼部病理检查显示眼球增大、巩膜变薄、房角和虹膜异常、睫状体和脉络膜发育不良以及晶状体原位较小。