{"title":"儿童期良性阵发性强直性上视;罕见的综合症","authors":"A. R. Galappaththi, J. Wanigasinghe","doi":"10.4038/CJMS.V54I1.4820","DOIUrl":null,"url":null,"abstract":"Benign Paroxysmal Tonic Upgaze is an oculomotor syndrome which was first described by Ovurier and Billson [1]. It consists of episodes of conjugate deviation of eyes with the onset in early infancy [2]. Detailed evaluation including metabolic, electroencephalographic and neuroimaging is often normal. The exact pathogenesis is yet unknown. We report a 10 month old boy who presented with persistent tonic upgaze.","PeriodicalId":253405,"journal":{"name":"Ceylon Journal of Medical Science","volume":"1990 2","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2017-06-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Benign paroxysmal tonic upgaze of childhood; a rare syndrome\",\"authors\":\"A. R. Galappaththi, J. Wanigasinghe\",\"doi\":\"10.4038/CJMS.V54I1.4820\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Benign Paroxysmal Tonic Upgaze is an oculomotor syndrome which was first described by Ovurier and Billson [1]. It consists of episodes of conjugate deviation of eyes with the onset in early infancy [2]. Detailed evaluation including metabolic, electroencephalographic and neuroimaging is often normal. The exact pathogenesis is yet unknown. We report a 10 month old boy who presented with persistent tonic upgaze.\",\"PeriodicalId\":253405,\"journal\":{\"name\":\"Ceylon Journal of Medical Science\",\"volume\":\"1990 2\",\"pages\":\"0\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2017-06-23\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Ceylon Journal of Medical Science\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.4038/CJMS.V54I1.4820\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Ceylon Journal of Medical Science","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.4038/CJMS.V54I1.4820","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Benign paroxysmal tonic upgaze of childhood; a rare syndrome
Benign Paroxysmal Tonic Upgaze is an oculomotor syndrome which was first described by Ovurier and Billson [1]. It consists of episodes of conjugate deviation of eyes with the onset in early infancy [2]. Detailed evaluation including metabolic, electroencephalographic and neuroimaging is often normal. The exact pathogenesis is yet unknown. We report a 10 month old boy who presented with persistent tonic upgaze.
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