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目标信号:与 RDH5 相关的眼底苍白点的多民族队列中的近红外特征和多模态成像。

THE TARGET SIGN: A Near Infrared Feature and Multimodal Imaging in a Pluri-Ethnic Cohort with RDH5-Related Fundus Albipunctatus.

机构信息

Ophthalmology Division, Tel Aviv Medical Center, Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.

Ruth & Bruce Rappaport Faculty of Medicine, Technion-Israel Institute of Technology, Haifa, Israel.

出版信息

Retina. 2022 Jul 1;42(7):1364-1369. doi: 10.1097/IAE.0000000000003466.

Abstract

PURPOSE

Retinol dehydrogenase 5 (RDH5)-related fundus albipunctatus can present with phenotypic variability. Our purpose was to investigate new clinical characteristics and multimodal imaging findings in patients from different ethnic origins, carrying different mutations.

METHODS

Multicenter international retrospective case series of 18 patients with genetically confirmed RDH5-related fundus albipunctatus. Patients' files were reviewed for fundus images, visual acuity, macular optical coherence tomography scans, near-infrared images, fundus autofluorescence, electroretinogram, and genetic mutations. Imaging and electroretinogram findings.

RESULTS

All eyes (n = 36, 100%) showed small circular findings seen on near-infrared images, termed as the "target sign," correlating to the yellowish dots seen clinically and to the distinct hyperreflective linear lesions on optical coherence tomography at the level between external limiting membrane and retinal pigment epithelium. Perifoveal atrophy with foveal sparing was seen in 4 eyes of 2 patients (both RDH5-c.160C>T, p.R54X mutation). Fundus autofluorescence revealed small hyperautofluorescent dots (n = 16, 44.4%). Scotopic electroretinograms were significantly reduced in all cases with an electronegative pattern, 66.7% displayed cone dysfunction.

CONCLUSION

Our results show distinct imaging findings present in all patients with fundus albipunctatus independent of ethnicity or genetic mutation. Our results can facilitate the current algorithm to diagnose RDH5-related fundus albipunctatus and allow for targeted genetic testing.

摘要

目的

视黄醇脱氢酶 5(RDH5)相关的眼底白点病可能表现出表型变异性。我们的目的是研究来自不同种族、携带不同突变的患者的新临床特征和多模态成像发现。

方法

对 18 名经基因证实的 RDH5 相关眼底白点病患者进行了多中心国际回顾性病例系列研究。对患者的病历进行了眼底图像、视力、黄斑光学相干断层扫描、近红外图像、眼底自发荧光、视网膜电图和基因突变的审查。

结果

所有眼睛(n=36,100%)均显示近红外图像上可见的小圆点状发现,称为“靶征”,与临床上所见的黄点状和光学相干断层扫描在外部限制膜和视网膜色素上皮之间的水平上所见的明显高反射线性病变相关。2 名患者的 4 只眼(均为 RDH5-c.160C>T,p.R54X 突变)出现了周边性萎缩伴中心凹保留。眼底自发荧光显示 16 只眼(44.4%)有小的高自发荧光点。暗适应视网膜电图在所有病例中均显著降低,呈电阴性模式,66.7%显示视锥功能障碍。

结论

我们的结果显示,所有眼底白点病患者均存在独特的影像学表现,与种族或基因突变无关。我们的结果可以促进当前诊断 RDH5 相关眼底白点病的算法,并允许进行有针对性的基因检测。

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