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隐匿性黄斑营养不良

Occult Macular Dystrophy.

作者信息

Sayman Muslubaş Işıl, Arf Serra, Hocaoğlu Mümin, Özdemir Hakan, Karaçorlu Murat

机构信息

İstanbul Retina Institute, İstanbul, Turkey.

出版信息

Turk J Ophthalmol. 2016 Apr;46(2):91-94. doi: 10.4274/tjo.26234. Epub 2016 Apr 5.

Abstract

Occult macular dystrophy is an inherited macular dystrophy characterized by a progressive decline of bilateral visual acuity with normal fundus appearance, fluorescein angiogram and full-field electroretinogram. This case report presents a 20-year-old female patient with bilateral progressive decline of visual acuity for six years. Her visual acuity was 3-4/10 in both eyes. Anterior segment and fundus examination, fluorescein angiogram and full-field electroretinogram were normal. She could read all Ishihara pseudoisochromatic plates. Fundus autofluorescence imaging was normal. There was a mild central hyporeflectance on fundus infrared reflectance imaging in both eyes. Reduced foveal thickness and alterations of the photoreceptor inner and outer segment junction were observed by optical coherence tomography in both eyes. Central scotoma was also found by microperimetry and reduced central response was revealed by multifocal electroretinogram in both eyes. These findings are consistent with the clinical characteristics of occult macular dystrophy.

摘要

隐匿性黄斑营养不良是一种遗传性黄斑营养不良,其特征是双侧视力进行性下降,而眼底外观、荧光素血管造影和全视野视网膜电图均正常。本病例报告介绍了一名20岁女性患者,其双侧视力进行性下降已有六年。她双眼视力均为3-4/10。眼前节和眼底检查、荧光素血管造影和全视野视网膜电图均正常。她能读出所有石原假同色图。眼底自发荧光成像正常。双眼眼底红外反射成像显示中央轻度低反射。光学相干断层扫描观察到双眼黄斑中心凹厚度变薄以及光感受器内外节交界处改变。双眼微视野检查也发现了中央暗点,多焦视网膜电图显示中央反应降低。这些发现与隐匿性黄斑营养不良的临床特征相符。

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