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首页> 外文期刊>Ophthalmic genetics >Hunter syndrome (MPS II-B): a report of bilateral vitreous floaters and maculopathy.
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Hunter syndrome (MPS II-B): a report of bilateral vitreous floaters and maculopathy.

机译：亨特综合征（MPS II-B）：双侧玻璃体漂浮症和黄斑病变的报告。

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PURPOSE: To describe bilateral vitreous opacities and maculopathy in a child with Hunter syndrome. METHODS: A case involving fundus examination, photography, and optical coherence tomography. Medline and Embase searches found no reference to vitreous or macular abnormalities in Hunter syndrome. RESULTS: A two-year-old boy with Hunter syndrome was found to have asymmetric, bilateral, free-floating vitreous opacities that remained stable over six years. Amblyopia and exotropia improved with occlusion therapy and spectacle correction. Visual acuity decreased when bilateral maculopathy supervened. CONCLUSION: Screening for vitreous abnormalities and maculopathy may be important in diagnosing, treating, and explaining visual loss in Hunter syndrome.
机译：目的：描述患有亨特综合征的儿童的双侧玻璃体混浊和黄斑病变。方法：一例涉及眼底检查，摄影和光学相干断层扫描。 Medline和Embase搜索未发现有关Hunter综合征的玻璃体或黄斑异常。结果：发现一名两岁男孩患有Hunter综合征，患有不对称，双侧，自由漂浮的玻璃体混浊，在六年内保持稳定。闭塞治疗和眼镜矫正可以改善弱视和散光。双侧黄斑病变取代后视力下降。结论：筛查玻璃体异常和黄斑病变可能对诊断，治疗和解释亨特综合征视力丧失具有重要意义。

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