R. Helton, K. Allen
{"title":"Acute Bilateral Retinal Arterial Occlusion of Unknown Origin during a Cystic Fibrosis Pulmonary Exacerbation","authors":"R. Helton, K. Allen","doi":"10.4172/2161-105X.1000481","DOIUrl":null,"url":null,"abstract":"Cystic fibrosis is a genetic disorder caused by a defective protein, cystic fibrosis transmembrane conductance regulator. The most common complications of this disease involve the pulmonary, gastrointestinal, and endocrine systems, though there are increasing reports of ocular complications related to cystic fibrosis. Here we report a case of a patient with bilateral retinal artery occlusion of unknown etiology. *Corresponding author: Richard Helton, Department of Pulmonology and Critical Care Medicine, University of Oklahoma, Oklahoma City, Oklahoma, USA, Tel: 5809270222; E-mail: richard-helton@ouhsc.edu Received December 10, 2018; Accepted December 20, 2018; Published December 27, 2018 Citation: Helton R, Allen K (2018) Acute Bilateral Retinal Arterial Occlusion of Unknown Origin during a Cystic Fibrosis Pulmonary Exacerbation. J Pulm Respir Med 8: 481. doi: 10.4172/2161-105X.1000481 Copyright: ©2018 Helton R, et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.","PeriodicalId":90449,"journal":{"name":"Austin journal of pulmonary and respiratory medicine","volume":"1 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2018-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Austin journal of pulmonary and respiratory medicine","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.4172/2161-105X.1000481","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
囊性纤维化肺恶化期间不明原因的急性双侧视网膜动脉闭塞
囊性纤维化是一种由囊性纤维化跨膜传导调节蛋白缺陷引起的遗传性疾病。该疾病最常见的并发症包括肺、胃肠和内分泌系统,尽管有越来越多的报道称与囊性纤维化相关的眼部并发症。我们在此报告一个病因不明的双侧视网膜动脉闭塞的病例。*通讯作者:Richard Helton,美国俄克拉何马州俄克拉何马市俄克拉何马大学肺病与重症医学系,电话:5809270222;邮箱:richard-helton@ouhsc.edu 2018年12月10日收稿;2018年12月20日录用;引用本文:Helton R, Allen K(2018)囊性纤维化肺恶化期间不明原因的急性双侧视网膜动脉闭塞。[J]中华肺科杂志8:481。2161 - 105 - x.1000481 doi: 10.4172 /版权所有:©2018 Helton R, et al。这是一篇根据知识共享署名许可协议发布的开放获取文章,该协议允许在任何媒体上不受限制地使用、分发和复制,前提是要注明原作者和来源。
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