Macular findings in Spectral Domain Optical Coherence Tomography and OCT Angiography in a patient with Kearns-Sayre syndrome.
Macular findings in Spectral Domain Optical Coherence Tomography and OCT Angiography in a patient with Kearns-Sayre syndrome.
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DOI：
10.1186/s40942-017-0077-8
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发表时间：
2017
影响因子：
2.3
通讯作者：
Ortiz J
中科院分区：
文献类型：
--
作者：
Ortiz A;Arias J;Cárdenas P;Villamil J;Peralta M;Escaf LC;Ortiz J
报告1例Kearns-Sayre综合征（KSS）的临床、电生理和解剖学表现。我们报告一例55岁女性KSS患者，其全身特征和眼部表现为眼肌麻痹和视网膜功能障碍，经电生理检查和高清晰度谱域光学相干断层扫描（HD SD OCT）和OCT血管造影（OCT-A）证实。我们报告了一例KSS患者，伴随着在外部HD SD OCT和OCT-A中观察到的RPE和光感受器的一些改变。据我们所知，这是文献中首次报告KSS患者的HD SD OCT结果。
To report the clinical, electrophysiological and the anatomical findings in a patient with Kearns–Sayre syndrome (KSS). We present the case of a 55-year-old female with KSS, who developed systemic features and ocular manifestations as ophthalmoplegia and retinal dysfunction, that were corroborated by electrophysiological test and High Definition Spectral Domain Optical Coherence Tomography (HD SD OCT) and OCT-Angiography (OCT-A). We report a patient with KSS, accompanied by some alterations of the RPE and photoreceptors observed in the external HD SD OCT and OCT-A. In the best of our knowledge, this is the first report in the literature of HD SD OCT findings in a patient with KSS.