{"title":"不寻常的关联：高铁蛋白血症和白内障","authors":"C. Guardo, Pia Esposto, Matteo Chinello","doi":"10.53126/mebxxvid218","DOIUrl":null,"url":null,"abstract":"Hyperferritinemia associated to cataract (HFC) is a rare genetic condition. In this report, the case of a 3 year old boy diagnosed with HFC is presented.","PeriodicalId":198715,"journal":{"name":"Medico e Bambino pagine elettroniche","volume":"21 6","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2023-12-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Un'insolita associazione: iperferritinemia e cataratta\",\"authors\":\"C. Guardo, Pia Esposto, Matteo Chinello\",\"doi\":\"10.53126/mebxxvid218\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Hyperferritinemia associated to cataract (HFC) is a rare genetic condition. In this report, the case of a 3 year old boy diagnosed with HFC is presented.\",\"PeriodicalId\":198715,\"journal\":{\"name\":\"Medico e Bambino pagine elettroniche\",\"volume\":\"21 6\",\"pages\":\"\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2023-12-22\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Medico e Bambino pagine elettroniche\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.53126/mebxxvid218\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Medico e Bambino pagine elettroniche","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.53126/mebxxvid218","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Un'insolita associazione: iperferritinemia e cataratta
Hyperferritinemia associated to cataract (HFC) is a rare genetic condition. In this report, the case of a 3 year old boy diagnosed with HFC is presented.
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