{"title":"[Vohwinkel综合征(附4例分析)]。","authors":"J Ocaña Sierra, G Blesa, E Montero","doi":"","DOIUrl":null,"url":null,"abstract":"<p><p>Four cases of keratoma hereditaria mutilans (Vohwinkel syndrome) are reported in two families, whereas clinic, metabolic, radiologic, histologic and cytogenetic aspects, the association with other processes, and therapeutic possibilities.</p>","PeriodicalId":75502,"journal":{"name":"Annales de dermatologie et de syphiligraphie","volume":"102 1","pages":"41-5"},"PeriodicalIF":0.0000,"publicationDate":"1975-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"[Vohwinkel's syndrome (study of 4 cases)].\",\"authors\":\"J Ocaña Sierra, G Blesa, E Montero\",\"doi\":\"\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Four cases of keratoma hereditaria mutilans (Vohwinkel syndrome) are reported in two families, whereas clinic, metabolic, radiologic, histologic and cytogenetic aspects, the association with other processes, and therapeutic possibilities.</p>\",\"PeriodicalId\":75502,\"journal\":{\"name\":\"Annales de dermatologie et de syphiligraphie\",\"volume\":\"102 1\",\"pages\":\"41-5\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"1975-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Annales de dermatologie et de syphiligraphie\",\"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":"Annales de dermatologie et de syphiligraphie","FirstCategoryId":"1085","ListUrlMain":"","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Four cases of keratoma hereditaria mutilans (Vohwinkel syndrome) are reported in two families, whereas clinic, metabolic, radiologic, histologic and cytogenetic aspects, the association with other processes, and therapeutic possibilities.
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