摘要
本文報告一位彼得氏複合症候群病例，患者為一位十七歲男性，眼部表徵為兩側先天性角膜中央後基質白斑，虹膜前黏連及輕度前極部白內障，且合併有顎裂畸形，輕度聽力障礙及智能不足，但兩眼視力約可達0.3左右，且患者已成年，故未給予任何處置。 彼得氏異常為一種少見的先天性前眼部的異常，可能合併其他系統異常，稱為彼得氏複合症候群。其致病機轉尚未定論，全層角膜移植效果不佳，玆就此加以討論之。
關鍵字
無資料並列摘要
We report a case of Peters' plus syndrome. This 17 year-old male presents typical Peters' anomaly associated with cleft palate, mild hearing loss and mental retardation. His vision has remained in the good condition, so no treatment was given. Peters' anomaly is a rare congenital abnormality that affects the anterior segment. Although the defect is limited to the eye, Peters' anomaly has been described in association with multi-systemic disorders. It has been called Peters' plus syndrome. The pat hogenesis is unclear and the outcome of management with penetrating keratoplasty not good.
延伸閱讀
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