Central retinal artery occlusion and subsequent amaurosis fugax in the contralateral eye associated with the G20210A prothrombin gene (F2) variant: a case report
Author:
Affiliation:
1. Neuroscience Research Group NeURos, Escuela de Medicina y Ciencias de la salud, Universidad del Rosario, Bogotá, Colombia
2. Escuela Superior de Oftalmología - Instituto Barraquer de América, Bogotá, Colombia
Funder
funding
Publisher
Informa UK Limited
Subject
Genetics (clinical),Ophthalmology,Pediatrics, Perinatology and Child Health
Link
https://www.tandfonline.com/doi/pdf/10.1080/13816810.2022.2068039
Reference37 articles.
1. FUNDUS CHANGES IN CENTRAL RETINAL ARTERY OCCLUSION
2. Retinal Artery OcclusionAssociated Systemic and Ophthalmic Abnormalities
3. A review of central retinal artery occlusion: clinical presentation and management
4. Central retinal artery occlusion
5. Lancellotti S, De Cristofaro R. Congenital prothrombin deficiency. Thieme Medical Publishers: © Thieme Medical Publishers, 2009:367–81.
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