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THE CLINICAL SEVERITY OF HEMOGLOBIN S / BLACK ((A)γδβ)(0)-THALASSEMIA
Hemoglobin S/Black ((A)γδβ)(0)-thalassemia is a rare sickle cell disease (SCD) variant. Based on limited descriptions in the literature, the disease is reported as a mild microcytic anemia with an uncomplicated course. We report the clinical and laboratory data of nine patients whose diagnoses were...
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| Publicat a: | Pediatr Blood Cancer |
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| Autors principals: | , , , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
2017
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6615052/ https://ncbi.nlm.nih.gov/pubmed/28453928 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/pbc.26596 |
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