{"title":"[Sickle cell hemoglobin C disease].","authors":"A. Lurie, J. Labeznik","doi":"10.32388/flec21","DOIUrl":null,"url":null,"abstract":"A hemoglobinopathy that is considered a hybrid of sickle cell disease and hemoglobin C disease. Patients present with the symptoms of sickle cell disease but the latter are less frequent and severe compared to sickle cell disease.","PeriodicalId":78205,"journal":{"name":"Dapim refuiim. Folia medica","volume":"25 1 1","pages":"131-7"},"PeriodicalIF":0.0000,"publicationDate":"2020-02-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"5","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Dapim refuiim. Folia medica","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.32388/flec21","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 5
Abstract
A hemoglobinopathy that is considered a hybrid of sickle cell disease and hemoglobin C disease. Patients present with the symptoms of sickle cell disease but the latter are less frequent and severe compared to sickle cell disease.