斜视导致阿伯特综合征的子午线弱视

S. Chowdhury, M. Srivastava, N. Chowdhury
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引用次数: 0

摘要

艾伯特综合症是一种非常罕见的疾病。大颅缝闭闭除了少见的特征外,其眼部特征也是主要的。这里报告的三个病例具有该综合征的典型特征。另外一例18岁女孩因外斜视而表现为子午线弱视。据我们所知,这是第一个病例报告,眼底图片证实存在外斜视的Apert 's综合征。第二例为凸出眼角膜糜烂,第三例为12岁女童,严重凸出伴颅缝闭锁及四肢并指。本报告的目的是显示该综合征在贾坎德邦的频率,并突出眼眶和面部畸形以及患者的严重并指畸形。
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Excyclotropia Leading to Meridoneal Amblyopia in Apert’s Syndrome
Apert’s syndrome is a very rare disease. Besides scarce features of acrocraniosynostosis, its ocular features are also predominant. Three cases, which are reported here, had typical features of the syndrome. Additionally one case of eighteen year old girl presented with meridoneal amblyopia due to excyclotropia. To our knowledge this is the first case report where fundus picture confirms presence of excyclotropia in Apert’s syndrome. Second case had corneal erosion in proptosed eyes and third case was of a 12 years girl with severe proptosis along with craniosynostosis and syndactyly of all four limbs. The purpose of this report is to show the frequency of this syndrome in Jharkhand and highlighting the orbital and facial deformities and severe syndactyly of patients.
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