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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| Format: | article |
| Langue: | EN |
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Wolters Kluwer Medknow Publications
2021
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| Accès en ligne: | https://doaj.org/article/2fd643919be34829aa60d2e577eba8e4 |
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