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A successful booster umbilical cord blood transplantation for a 10-year-old patient with beta-thalassemia major in India
Beta-thalassemia major is characterized by a genetic deficiency in synthesis of beta-globin chains, resulting in reduced levels of functional hemoglobin. It is characterized by anemia, hepatosplenomegaly, and iron overload due to repeated blood transfusion. Hematopoietic stem cell transplantation is...
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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Wolters Kluwer - Medknow
2021
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8628234/ https://www.ncbi.nlm.nih.gov/pubmed/34908765 http://dx.doi.org/10.4103/ajts.ajts_109_20 |