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Optical coherence tomography and fundus autofluorescence imaging study of chorioretinal atrophy involving the macula in Alagille syndrome

机译:光学相干断层扫描和眼底自体荧光成像研究Alagille综合征涉及黄斑的脉络膜视网膜萎缩

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Abstract: We report the first case in the literature of chorioretinal atrophy involving the macula in an 11-year-old girl with Alagille syndrome, as examined by optical coherence tomography, and fundus autofluorescence imaging. Funduscopy revealed diffuse choroidal hypopigmentation with increased visibility of the choroidal vessels and symmetric, well circumscribed macular discoloration. Anomalous oblique configuration of the optic disc and peripapillary tortuous vessels were also detected. Optical coherence tomography demonstrated decreased retinal thickness, especially the outer retinal layer, and the photoreceptor inner segment/outer segment junctions were irregular and discontinued, corresponding to macular discoloration. Fundus autofluorescence imaging clearly defined hypofluorescent areas in the peripapillary regions that extended along the macula and had a sleep mask appearance. We suggest that transient hypovitaminosis due to Alagille syndrome early in life might contribute to the retinal degeneration seen in this case.
机译:摘要:通过光学相干断层扫描和眼底自发荧光成像检查,我们报道了11例患有Alagille综合征的女孩的视网膜黄斑萎缩累及黄斑。眼底镜检查显示出脉络膜色素沉着弥漫性不全,脉络膜血管的可见度增加,对称性,界限清楚的黄斑变色。还检测到视盘和乳头周围曲折血管的异常倾斜配置。光学相干断层扫描显示视网膜厚度减少,尤其是视网膜外层,并且感光器内部节段/外部节段连接处不规则且不连续,对应于黄斑变色。眼底自发荧光成像清楚地定义了沿黄斑延伸并具有睡眠面罩外观的乳突周周围区域的低荧光区域。我们建议,在这种情况下,生命早期因Alagille综合征而导致的短暂性维生素缺乏症可能会导致视网膜变性。

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