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A Rare Case of Unilateral Morning Glory Disc Anomaly in a Patient with Turner Syndrome: Report and Review of Posterior Segment Associations

机译:特纳综合征患者单侧晨光碟异常的罕见病例:后节协会的报告和审查

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摘要

Turner syndrome is a common sex chromosome disorder affecting females. The disorder is caused by a partial loss, complete absence, or structural abnormality of one X chromosome. The clinical presentation is broad and ranges from the classic phenotype to minimal clinical manifestations. Ocular abnormalities associated with the syndrome are common. Reports describing abnormal eye features in individuals with Turner syndrome generally involve refractive errors (myopia or hyperopia), strabismus, and external or anterior segment abnormalities including hypertelorism, epicanthal folds, and ptosis. Posterior ocular segment anomalies involving the optic nerve and retina in Turner syndrome have been rarely reported. We report a rare presentation of an 11-year-old female with Turner syndrome and unilateral morning glory disc anomaly.
机译:特纳综合征是一种影响女性的常见性染色体疾病。该疾病是由一个X染色体的部分丢失,完全缺失或结构异常引起的。临床表现广泛,范围从经典表型到极少的临床表现。与综合征相关的眼部异常很常见。描述特纳综合症患者眼部功能异常的报告通常涉及屈光不正(近视或远视),斜视以及外部或前段异常,包括眼肌过度,上can褶和上睑下垂。特纳综合征中涉及视神经和视网膜的眼后段异常很少见报道。我们报告罕见地介绍了一名11岁的特纳综合征和单侧牵牛花盘异常的女性。

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