EF Bart's Disease with Coinheritance of Gγ-XmnI and Aγ-Globin Polymorphisms: A Case of Nontransfusion-Dependant Thalassemia

EF Bart's disease is a rare form of nontransfusion-dependant thalassemia (NTDT) due to the coinheritance of homozygous hemoglobin E (β(E)/β(E)) genotype with hemoglobin H disease. These individuals are routinely found to have thalassemia intermedia with moderate anemia, increased hemoglobin Bar...

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書目詳細資料
發表在:Case Rep Hematol
Main Authors: Laks, Kane M., Hirner, Cara, Gruner, Barbara, Coberly, Jared, Laziuk, Katsiaryna, Sathi, Bindu Kanathezhath
格式: Artigo
語言:Inglês
出版: Hindawi 2020
主題:
Case Report
在線閱讀:https://ncbi.nlm.nih.gov/pmc/articles/PMC7647742/
https://ncbi.nlm.nih.gov/pubmed/33178467
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1155/2020/8869335
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