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Paediatric Bone Marrow Transplant

Paediatric Bone Marrow Transplant
World-renowned bone marrow transplant specialists pioneering new techniques
High-volume centre for half-match transplants matching international success rate
State-of-the-art centre with 24x7 blood bank support, advanced infrastructure
Expertise in HLA-matching techniques optimising donor compatibility
Dedicated paediatric team, PICU and multi-disciplinary support for complex illnesses
Among top care centres for relapse or refractory blood cancer in children

The Medanta Paediatric BMT Division is dedicated to improving the lives of children with blood disorders like Thalassemia, cancers, immune disorders. We are driven to offer hope to parents and add life to years for our young patients through innovative curative treatments.

Satya Prakash Yadav
Dr. Satya Prakash Yadav
Director
‘Boosting immunity, changing lives’
Transforming the Future Through Marrow Transplants
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Our division is led by a team of doctors who have pioneered many BMT procedures in the world and India

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We specialise in catering to children suffering from thalassemia, sickle cell disease, cancers, immunodeficiency disorders of the blood

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Expertise in half-match BMT, unrelated cord blood transplant and cell therapies that are not widely available, like CAR-T cell therapy

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Our multidisciplinary approach ensures children get holistic and the gentlest treatment possible to ensure they continue to meet growth milestones

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At Medanta, we currently averages 100 paediatric BMTs each year, making us a high-volume centre, driven to achieve excellence

Boosting immunity, changing lives : Bone marrow transplant specialists and surgeons at your disposal
Our Ailments
Inherited Blood Disorders
Thalassemia

Inherited blood disorders such as Thalassemia and Sickle Cell Disease (SCD) significantly impact the production and function of haemoglobin, the protein in red blood cells responsible for oxygen transport. Thalassemia affects the body's ability to produce haemoglobin. There are two main types: alpha and beta-thalassemia. The severity of symptoms varies depending on the type and number of gene mutations inherited. Individuals may experience mild to severe anaemia, leading to symptoms like fatigue, weakness, and shortness of breath. Management includes regular blood transfusions and chelation therapy to remove excess iron from the body. SCD is a group of inherited disorders that cause abnormal haemoglobin. The most common form is Sickle Cell Anaemia. In SCD, red blood cells become sickle-shaped, stiff, and sticky, leading to a shortage of healthy red blood cells. These sickle cells can block blood flow in small vessels, causing severe pain and complications such as infections, acute chest syndrome, and stroke. Both Thalassemia and SCD can be cured with Bone Marrow Transplant to improve quality of life and longevity.

Primary immunodeficiency
Primary immunodeficiency

Primary immunodeficiency disorders (PI) are a group of over 300 genetic disorders that impair the immune system’s ability to defend against infections. Individuals with PI have defects in the cells or proteins that make up the immune system, leading to frequent, severe, or unusual infections. Symptoms can range from mild to severe and may include recurrent respiratory infections, gastrointestinal issues, skin infections, and failure to thrive in infants. Diagnosing PI often involves a combination of clinical evaluation, family history, and specialized laboratory tests. Treatment varies depending on the specific disorder but may include immunoglobulin replacement therapy, antibiotics to prevent and treat infections, and in some cases, hematopoietic stem cell transplantation to correct the underlying immune defect.

Leukaemia
Leukaemia

Leukaemia is a type of blood cancer that affects the white blood cells. It primarily starts in the bone marrow, the site where blood cells are produced. The most common types of leukaemia acute lymphoblastic leukaemia (ALL), acute myeloid leukaemia (AML), and chronic myeloid leukaemia (CML). It is crucial to consult a doctor for accurate diagnosis and treatment options specific to the type you might have.

Aplastic Anaemia
Aplastic Anaemia

Aplastic anaemia is a rare but serious disorder that disrupts the bone marrow's ability to produce enough blood cells. This malfunctioning bone marrow leads to deficiencies in red blood cells (causing fatigue), white blood cells (increasing infection risk), and platelets (raising the risk of bleeding). Aplastic anaemia has no universal cure, but treatments like blood transfusions and medications can help manage symptoms. In some cases, a stem cell transplant may offer a potential cure.

Latest Technology
CD45RA Depletion
CD45RA Depletion

CD45RA Depletion is a specialised technique used in allogeneic hematopoietic stem cell transplantation and cell therapy. CD45RA is a marker found on naïve T cells, which have not yet encountered antig..

Blood and Bone Marrow Stem Cell Collection
Blood and Bone Marrow Stem Cell Collection

Whether you are a donor or need an allogeneic transplant, blood stem cells can be collected from your bloodstream or bone marrow. While the largest concentration of stem cells is in the bone marrow,..

TCR Alpha-Beta Depletion
TCR Alpha-Beta Depletion

TCR Alpha-Beta Depletion is an advanced technique used in haematopoietic stem cell transplantation (HSCT) to enhance the safety and efficacy of the procedure. T-cell receptors (TCRs) are proteins foun..

CAR T Cell Therapy
CAR T Cell Therapy

Chimeric Antigen Receptor (CAR) T cell therapy is a highly personalised, targeted and effective therapeutic approach for half-match transplantation and cancer. It involves genetically modifying a pati..

Donor Lymphocyte Infusion
Donor Lymphocyte Infusion

Donor Lymphocyte Infusion (DLI) is a valuable procedure in the post-transplant management of patients, supporting overall immune recovery, and fighting residual cancer cells and relapse. It involves i..

Doctors, Pioneers, Life Savers

Our superspecialist doctors provide the highest quality of care through a team-based, doctor-led model. Trained at some of the world's most renowned institutions, our highly experienced doctors are distinguished experts in their respective specialities. Our doctors work full-time and exclusively across Medanta hospitals. In addition to offering superspecialised care in their own field, the Medanta organisational structure enables every doctor to help create a culture of collaboration and multispecialty care integration.

Our superspecialist doctors provide the highest quality of care through a team-based, doctor-led model. Trained at some of the world's most renowned i..... Continue Reading

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