{"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}
引用次数: 0
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.
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