OPTIC DISK COLOBOMA MAY TRIGGER MULTIPLE EVANESCENT WHITE DOT SYNDROME: EXPANDING THE CLINICAL SPECTRUM [0.03%]
视盘胶质瘤可能是多发性短暂白点综合征的诱因：扩大临床谱系范围的新见解
Abdulrahman F AlBloushi,Sarah Mohammed Almuwarraee,Fadwa Al Adel
Abdulrahman F AlBloushi
Purpose: To report a case of secondary multiple evanescent white dot syndrome (MEWDS) that occurred in a patient with optic disk coloboma. Methods: ...
COMBINED CENTRAL RETINAL ARTERY AND VEIN OCCLUSION-LIKE MANIFESTATIONS WITH APLASTIC ANEMIA: UNVEILING PATHOPHYSIOLOGICAL INSIGHTS [0.03%]
结合中心性视网膜动脉和静脉阻塞样表现的再生障碍性贫血：揭示病理生理机制
Carlos Rodrigo Damasceno Feitosa de Santana,Felipe de Queiroz Tavares Ferreira
Carlos Rodrigo Damasceno Feitosa de Santana
Purpose: To report the association of a combined central artery and vein occlusion-like pattern with aplastic anemia and discuss the pathophysiology associated with ophthalmologic examinations. ...
Victoria A Marks,Vijitha S Vempuluru,Carol L Shields
Victoria A Marks
Purpose: We report a rare case of systemic Hodgkin lymphoma with presumed intraocular involvement that resolved after systemic chemotherapy. Methods: ...
DIET-INDUCED RESOLUTION OF MACULAR OEDEMA FOLLOWING REMISSION OF TYPE 2 DIABETES MELLITUS IN A PATIENT UNDERGOING THERAPEUTIC CARBOHYDRATE REDUCTION [0.03%]
低碳饮食治疗2型糖尿病缓解后黄斑水肿的消退：一例报告
Lewis R Hains,Stephen Bacchi,Rachelle Martin et al.
Lewis R Hains et al.
Purpose: There is growing evidence to support the potential role of low-carbohydrate healthy fat and ketogenic diets (therapeutic carbohydrate reduction - therapeutic carbohydrate reduction) in the management of diabetes ...
LEBER HEREDITARY OPTIC NEUROPATHY: A CASE REPORT OF CONCURRENT RARE MITOCHONDRIAL MUTATIONS AND ABCA4 NUCLEAR GENE MUTATION [0.03%]
线粒体基因和核基因突变共存导致的莱伯遗传性视神经病一例报告
Maryam Ashrafkhorasani,Brian Chou,Alfredo A Sadun
Maryam Ashrafkhorasani
Purpose: This case report aimed to describe the clinical presentation of a 21-year-old male patient with subacute bilateral painless vision loss, clinically consistent with Leber hereditary optic neuropathy (LHON), a mito...
WHEN TUBERCULIN STINGS: A CASE OF PANOPHTHALMITIS FOLLOWING TUBERCULIN SKIN TEST [0.03%]
结核菌素皮试后发生全葡萄膜炎的病例报告
Anindya Kishore Majumder,Parthopratim Dutta Majumder
Anindya Kishore Majumder
Purpose: The objective of this study was to report a case of allergic reaction to a tuberculin skin test that incited a panophthalmitis-like reaction with exudative retinal detachment. ...
MIDPERIPHERAL RETINAL THICKENING ON WIDEFIELD OPTICAL COHERENCE TOMOGRAPHY IN A PATIENT WITH A MUTATION IN THE NR2E3 GENE [0.03%]
携带NR2E3基因突变患者的广域光学相干断层扫描下的周边视网膜增厚
Jan Willem R Pott,E Angela Huiskamp,Joke B G M Verheij
Jan Willem R Pott
Purpose: To report typical retinal findings in a girl with the presumed diagnosis of enhanced S-cone syndrome, attributed to the presence of a homozygous likely pathogenic variation in the NR2E3 gene. ...
Katrin Fasler,Eléonore Multone,Marc Stahel et al.
Katrin Fasler et al.
Purpose: The aim of this study was to describe a case of vitreous amyloidosis as a rare aetiology of vitreous opacities and to show diagnostic value of vitreous biopsy in the diagnostic process as well as show a potientia...
Coloboma associated with VACTERL characterized by Ultra-Widefield Optical Coherence Tomography [0.03%]
超宽域光学相干断层扫描(VACTERL并列结膜和角膜缺损)
David A Sutter,Yakub A Bayhaqi,Shuibin Ni et al.
David A Sutter et al.
Purpose: To describe an infant with VACTERL syndrome with a concomitant iris and chorioretinal coloboma, imaged with ultra-widefield optical coherence tomography (UWF-OCT). ...
Aruba Zafar,YuBai Chou,Carol L Shields
Aruba Zafar