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首页> 外文期刊>Journal of pediatric genetics >A Case of Anterior Segment Dysgenesis with Iridolenticular Adhesions in Trisomy 18
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A Case of Anterior Segment Dysgenesis with Iridolenticular Adhesions in Trisomy 18

机译：三元18中具有虹折性粘连的前段性脱节的情况

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Trisomy 18 (or Edwards syndrome) has an incidence of 1 in 6,000 to 8,000 live births, making it the second most common trisomy after trisomy 21. Ophthaimologic anomalies include epicanthal folds, hypertelorism, and hypoplastic supraorbital ridges, whereas corneal opacities, microcornea, congenital glaucoma, cataract, retinal depig-mentation, retinal vascular tortuosity, colobomatous microphthalmia, and cyclopia are thought to be less common; iridolenticular adhesions have not been previously reported. Our patient was a female with confirmed trisomy 18 with ophthaimologic examination revealing corneal opacities and iridolenticular adhesions. Insofar as corneal opacities are a known entity in trisomy 18 and have been considered by some to be of clinical importance, iridolenticular adhesions may also be a noteworthy manifestation of the disease's anterior segment dysgenesis.
机译：三兆癣18（或Edwards综合征）的发病率为6,000至8,000个活产，使其成为三术后的第二个最常见的三颗粒。眼神异常包括癫痫折叠，高度兴奋剂和软骨缺水脊，而角膜不透明，先天性，先天性 青光眼，白内障，视网膜诊断，视网膜血管曲屈曲折，小区血栓性微蛋白和环族被认为不太常见; 之前尚未报道铱星形粘连。 我们的患者是一名女性，具有证实的三元图18，具有眼压检查，揭示角膜不透明和虹膜凝固粘连。 少数角膜不透明度是三元18中的已知实体，并被一些人认为是临床重要性，铱星形粘连也可能是疾病的前段性疾病的值得注意的表现。

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