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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Detalles Bibliográficos
Autores principales: Laks, Kane M., Hirner, Cara, Gruner, Barbara, Coberly, Jared, Laziuk, Katsiaryna, Sathi, Bindu Kanathezhath
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2020
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7647742/
https://www.ncbi.nlm.nih.gov/pubmed/33178467
http://dx.doi.org/10.1155/2020/8869335

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7647742/
https://www.ncbi.nlm.nih.gov/pubmed/33178467
http://dx.doi.org/10.1155/2020/8869335

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