Thalassemia is an inherited blood disorder, in this condition the body makes an abnormal form of hemoglobin. The Hemoglobin is the protein molecule in red blood cell that carries oxygen through the blood vessels. This disorder results in excessive destruction of red blood cells (RBSc) of the individual and this is what leads to anemia. For you know know what is Anemia is very important, This Anemia is a condition/situation in which the human body does not have enough normal and healthy red blood cells.
The Allogenic transplant (Stem cells taken from donor) is the procedure which is required to be done in patients suffering from thalassemia disease in which bone marrow cells are received from a HLA matched donor, these stem cells are later infused to the recipient (Patient) for the marrow to begin producing normal red blood cells and other cells also and stop forming abnormal blood cells which are not normal. This procedure is offered to patients who regularly require blood transfusion and this allogenic transplant is planned for those patients who are considered eligible for it considering all the clinical aspects and patient’s condition. Please note that all the patients suffering from thalassemia disease are not candidates of bone marrow transplant. Some of the Patients do well with other therapies offered at top hospitals like BLK-MAX Super Speciality Hospital, Apollo Hospitals, Fortis Hospitals, Artemis Hospitals and American Oncology Institute etc.
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