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β-thalassemia caused by compound heterozygous mutations and cured by bone marrow transplantation: A case report
In the present study, a rare familial case of severe thalassemia with compound spontaneous mutations is reported. A 2.5-year-old boy, who suffered from severe anemia with yellowish skin, enlarged liver and spleen, was provided with a blood transfusion every 20 days to maintain hemoglobin levels betw...
| Autores principales: | , , , , , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
D.A. Spandidos
2017
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5865824/ https://www.ncbi.nlm.nih.gov/pubmed/28901454 http://dx.doi.org/10.3892/mmr.2017.7476 |