{"title":"Un caso di anemia macrocitica non megaloblastica: la sindrome di Blackfan Diamond","authors":"Giulia Aquisti, Maria Eleonora Basso, I. Rabbone","doi":"10.53126/mebxxviimg92","DOIUrl":null,"url":null,"abstract":"The case of a two-year-old child with severe isolated anaemia (6 g%) and marked macrocytosis, ultimately diagnosed as Blackfan-Diamond syndrome, is described. The genetic, clinical and prognostic aspects of the disease are briefly discussed.","PeriodicalId":198715,"journal":{"name":"Medico e Bambino pagine elettroniche","volume":"4 12","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2024-05-24","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/mebxxviimg92","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
The case of a two-year-old child with severe isolated anaemia (6 g%) and marked macrocytosis, ultimately diagnosed as Blackfan-Diamond syndrome, is described. The genetic, clinical and prognostic aspects of the disease are briefly discussed.