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Pediatric Keratoprosthesis: A New Surgical Approach

机译:小儿角膜塑形术:一种新的手术方法

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INTRODUCTION FROM THOMAS JOHN, MD:A number of genetic, developmental, metabolic and idiopathic causes can result in congential clouding of the cornea. These include Peters anomaly, sclerocornea, dermoid, primary congenital glaucoma, birth trauma, congenital central corneal leukoma, congenital hereditary endothelial dystrophy, posterior polymorphous dystrophy, mucopolysacharidosis, infectious/inflammatory processes, corneal keloid, congenital hereditary stromal dystrophy, and other causes. Treatment is primarily surgical. In the pediatric age group, when there is bilateral and visually disabling corneal opacity, a penetrating keratoplasty (PKP) is usually the treatment of choice. In order to prevent amblyopia, the earlier the PKP is performed (usually prior to 3-6 months of age) the better the visual results. However, in the pediatric age group, PKP is a high-risk surgical procedure.
机译:医学博士THOMAS JOHN的介绍:许多遗传,发育,代谢和特发性病因都可能导致角膜的持续浑浊。这些包括彼得斯异常,巩膜炎,皮肤样皮炎,原发性先天性青光眼,出生创伤,先天性中央角膜白细胞瘤,先天性遗传性内皮营养不良,后部多形营养不良,粘膜多糖代谢异常,感染性/炎性过程,角膜瘢痕loid,先天性遗传性间质。治疗主要是外科手术。在小儿年龄组中,当双侧视障角膜混浊时,通常选择穿透性角膜移植术(PKP)。为了预防弱视,PKP越早执行(通常在3-6个月大之前),视觉效果越好。但是,在小儿年龄段,PKP是高风险的外科手术。

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