{"title":"[Urbach-Wieth综合征]。","authors":"C Charlin, F L Fernandez","doi":"","DOIUrl":null,"url":null,"abstract":"<p><p>The \"Urbach-Wiethe syndrom\" is an hereditary disease which start during early childhood, distinguishable by a lipoglycoproteinosis which affects the skin, mucosae and also the eyes, with cyst formations in the lid's marginal, drusen of Bruch's membrane. Corneal opacities, and glaucoma seen to be rarer.</p>","PeriodicalId":75539,"journal":{"name":"Archives d'ophtalmologie et revue generale d'ophtalmologie","volume":"35 6-7","pages":"521-6"},"PeriodicalIF":0.0000,"publicationDate":"1975-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"[Urbach-Wiethe syndrome].\",\"authors\":\"C Charlin, F L Fernandez\",\"doi\":\"\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>The \\\"Urbach-Wiethe syndrom\\\" is an hereditary disease which start during early childhood, distinguishable by a lipoglycoproteinosis which affects the skin, mucosae and also the eyes, with cyst formations in the lid's marginal, drusen of Bruch's membrane. Corneal opacities, and glaucoma seen to be rarer.</p>\",\"PeriodicalId\":75539,\"journal\":{\"name\":\"Archives d'ophtalmologie et revue generale d'ophtalmologie\",\"volume\":\"35 6-7\",\"pages\":\"521-6\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"1975-06-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Archives d'ophtalmologie et revue generale d'ophtalmologie\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Archives d'ophtalmologie et revue generale d'ophtalmologie","FirstCategoryId":"1085","ListUrlMain":"","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
The "Urbach-Wiethe syndrom" is an hereditary disease which start during early childhood, distinguishable by a lipoglycoproteinosis which affects the skin, mucosae and also the eyes, with cyst formations in the lid's marginal, drusen of Bruch's membrane. Corneal opacities, and glaucoma seen to be rarer.