Sickle Cell Anemia is a severe blood disorder in which red blood cells become abnormal in shape and lose their ability to supply oxygen throughout the body.
In mild cases, Sickle Cell Anemia treatment requires medication and blood transfusions.
In rare cases, it may need a bone marrow transplant.
Listing approximate price of Sickle Cell Anemia Treatment and some related procedures. The prices may change depending upon the centers and condition of the patient.
Treatment name | Cost range |
---|---|
Bone Marrow Transplant | Rs.666000 to Rs.888000 |
Popular Hospitals in Delhi ncr for Sickle Cell Anemia Treatment are:
The right doctor to consult for Sickle Cell Anemia is a Hematologist who specializes in treating blood disorders.
Listing popular specialists:
Senior Consultant, 23 years of experience
Hematology and Bone Marrow Transplantation
Consultant, 14 years of experience
Bone Marrow Transplant & Haematology
Senior Consultant, 23 years of experience
Marrow Transplantation
Chairman, 28 years of experience
<p>Bone Marrow Transplant, Hemato-Oncology Graft Versus Host Disease Allogenic Bone Marrow Transplant, High-risk Thalassemia Major with a new conditioning regimen</p>
Consultant, 15 years of experience
Thalassemia & Aplastic Anemia, Hematology, Bone Marrow Transplant
Senior Consultant, 6 years of experience
Hematology
HOD, 10 years of experience
Neoplastic Flow cytometry, Molecular hematology, HLA and hemostasis
Senior Consultant, 21 years of experience
Benign Paediatric haematology Haemato-oncology Matched sibling and unrelated and Paediatric haploidentical transplants
Senior Consultant, 23 years of experience
Oncology, Organ Transplant Pediatric hemato-oncology Bone marrow transplant
Director, 16 years of experience
Blood Transfusion, Bone Marrow Transplant, Chelation Therapy, Lymphatic drainage, Thalassaemia, Haemophilia, Biochemistry
Associate Director, 16 years of experience
Hemato-oncology, Haemophilia
Consultant, 13 years of experience
Brain and bone tumors, Lymphomas, Leukemias, Solid Tumors, Bone Marrow Transplant, Clotting disorders, Anemias
Consultant, 25 years of experience
Haemato-Oncology Leukaemia Acute Leukaemia (AML/ ALL) Lymphoma Multiple Myeloma Bone Marrow Transplant CML CLL Chronic Myeloproliferative Neoplasm Myelodysplastic syndrome Anemia Thalassemia Bleeding and clotting disorders Induction therapies for acute leukemia
Senior Consultant, 19 years of experience
Lymphoma Myeloma Thalassemia Aplastic anemia.
Consultant, 14 years of experience
Allogeneic Transport for Leukemia Haplo - Identical Stem Cell Transplant Cellular Therapy
Senior Consultant, 20 years of experience
Matched Sibling donor Stem cell transplant Matched Unrelated Donor Stem cell Transplant Haematological disorders including Aplastic Anemia and Thalassemia Major
Consultant, 19 years of experience
Autologous BMT for Multiple Myeloma Allogenic BMT for benign disorders like Thalassemia, Sickle cell anaemia, Aplastic anemia, and bone marrow failure syndromes. Hemophilia & bleeding disorders Hemaglobinopathies
Senior Consultant, 14 years of experience
Leukemia Lymphoma Thalassemia Coagulation Disorders Bone Marrow Transplant
Consultant, 15 years of experience
Autologous Stem cell Transplant Matched Sibling Allogenic Stem cell Transplant Haplo Identical Stem cell Transplant Matched Unreletaed Donor Transplant Bone Marrow Aspiration & Biopsy Lumbar Puncture with Intrathecal Chemo Benign and Malignant Hematological Blood Disorder
With improvements in diagnosis and medical care, the success rate of Sickle Cell Anemia is above 95%.
Some symptoms of Sickle Cell Anaemia may include -
Our Services for Sickle Cell Anemia Treatment in Delhi Ncr
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Sickle cell anemia is an inherited red blood cells disorders in which the red blood cells are not healthy enough to carry oxygen through the body, red blood cells can easily move throughout the blood vessels.
can get sickle cell anemia from when you inherit sickle cell from both your parents. When both your parents are carriers of sickle cell gene then you can get sickle cell anemia.
The organs affected by sickle cell anemia are the liver, heart, kidney, gallbladder, eyes, bones and joints. It can cause recurrent infections, symptoms of sickle cell anemia usually appear 5 months of age. Some of the symptoms of sickle cell anemia includes anemia, episodes of pain, swelling in hands and feet, fever, pale skin, frequent infections etc.
If both mother and father are carrier then child may get affected from sickle cell anemia.
Complications of sickle cell anemia includes stroke, acute chest syndrome, pulmonary hypertension, organ damage, blindness, ulcers in leg, gall bladder stone and pulmonary hypertension.
Sickle cell anemia is being diagnosed by blood test, blood test checks for the defective form of hemoglobin causes sickle cell anemia. Adults and children can also be tested or sickle cell anemia.
Sickle cell anemic avoids the episodes of pain, relieves the symptoms and prevents complication. The treatment of sickle cell anemia included medications and blood transfusion.
The surgical procedure of sickle cell anemia involves blood transfusion, in red blood cell transfusion red blood cells are being removed from the supply of donated blood. This increases the supply of red blood cells.
Blood transfusion takes around 90 to 120 minutes to be completed and it can even be done in smaller children who are younger than 5 years.
The process of stem cell transplant usually takes around 3 weeks to be done.
Stem cell transplant is also known as bone marrow transplant the process of stem cell transplant involves replacing the bone marrow of the affected person with the healthy bone marrow of the donor.
Stem cell transplant involves long hospital stay, after getting transplant you will need to get drug for preventing rejection of the donated stem cells. In some cases, your body may reject the transplant which may result in some life-threatening complications.
If you have sickle cell anemia by seeing a genetic counselor before you trying to conceive will help you in understanding the risk of having a child with sickle cell anemia.
Red blood cells usually live for about 120 days before they need to be replaced. But sickle cells usually die in 10 to 20 days, leaving a shortage of red blood cells,.
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