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Thalassemia Treatment in India

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Recommended Doctors for Thalassemia View All View All

Dr Rahul Bhargava
Dr Rahul Bhargava

Director - Blood Disorders And Bone Marrow Transplant

CONSULTS AT

Fortis Memorial Research Institute, Gurgaon +1

EXPEREIENCE :
15 years
SURGERIES :
800+

Treatment Price on request

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Treatment Price on request

Dr Rahul Bhargava
Dr Rahul Bhargava

Director - Blood Disorders And Bone Marrow Transplant

CONSULTS AT

Fortis Memorial Research Institute, Gurgaon +1

EXPEREIENCE :
15 years
SURGERIES :
800+
Dr. Dharma Choudhary
Dr. Dharma Choudhary

Director & Senior Consultant - Deptt. Of Bone Marrow Transplant

CONSULTS AT

BLK-Max Super Speciality Hospital, New Delhi +1

EXPEREIENCE :
20 years
SURGERIES :
NA

Treatment Price on request

Free Text Consult

Treatment Price on request

Dr. Dharma Choudhary
Dr. Dharma Choudhary

Director & Senior Consultant - Deptt. Of Bone Marrow Transplant

CONSULTS AT

BLK-Max Super Speciality Hospital, New Delhi +1

EXPEREIENCE :
20 years
SURGERIES :
NA
Dr Vikas Dua
Dr Vikas Dua

Additional Director & Hod - Blood Disorders And Bone Marrow Transplant

CONSULTS AT

Fortis Memorial Research Institute, Gurgaon +1

EXPEREIENCE :
21 years
SURGERIES :
200+

Treatment Price on request

Free Text Consult

Treatment Price on request

Dr Vikas Dua
Dr Vikas Dua

Additional Director & Hod - Blood Disorders And Bone Marrow Transplant

CONSULTS AT

Fortis Memorial Research Institute, Gurgaon +1

EXPEREIENCE :
21 years
SURGERIES :
200+
Dr. Neha Rastogi
Dr. Neha Rastogi

Senior Consultant - Medical And Haemato Oncology , Cancer Institute

CONSULTS AT

Medanta - The Medicity

EXPEREIENCE :
14 years
SURGERIES :
NA

Treatment Starting at $37,000

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Treatment Starting at $37,000

Dr. Neha Rastogi
Dr. Neha Rastogi

Senior Consultant - Medical And Haemato Oncology , Cancer Institute

CONSULTS AT

Medanta - The Medicity

EXPEREIENCE :
14 years
SURGERIES :
NA
Dr. Satya Prakash Yadav
Dr. Satya Prakash Yadav

Director - Paediatric Hemato Oncology & Bone Marrow Transplant Medical And Haemato Oncology , Cancer Institute

CONSULTS AT

Medanta - The Medicity

EXPEREIENCE :
15 years
SURGERIES :
NA

Treatment Starting at $37,000

Free Text Consult

Treatment Starting at $37,000

Dr. Satya Prakash Yadav
Dr. Satya Prakash Yadav

Director - Paediatric Hemato Oncology & Bone Marrow Transplant Medical And Haemato Oncology , Cancer Institute

CONSULTS AT

Medanta - The Medicity

EXPEREIENCE :
15 years
SURGERIES :
NA
Dr. Gaurav Dixit
Dr. Gaurav Dixit

​unit Head - Haemato Oncology (unit Ii)

CONSULTS AT

Artemis Hospital

EXPEREIENCE :
11+ years
SURGERIES :
NA

Treatment Price on request

Free Text Consult

Treatment Price on request

Dr. Gaurav Dixit
Dr. Gaurav Dixit

​unit Head - Haemato Oncology (unit Ii)

CONSULTS AT

Artemis Hospital

EXPEREIENCE :
11+ years
SURGERIES :
NA

Thalassemia Treatment In India
  1. The total cost of thalassemia treatment in India starts from USD 30000.
  2. The success rate of thalassemia treatment in India is almost 70 percent
  3. The top hospitals for thalassemia treatment in India are Fortis Gurgaon, Dharamshila Narayana and BLK Hospital. The best doctors in the field are Dr. Rahul Bhargava, Dr. Suparno Chakrabarti, and Dr. Dharma Chaudhary.
  4. The patient needs to stay for almost 90 days in India for thalassemia treatment.
About Thalassemia treatment

Thalassemia is a condition of a genetic blood disorder in which a person is highly anemic because of the low production of hemoglobin in the body. Due to the lack of hemoglobin production in the body, the Red Blood Cells (RBCs) are unable to carry enough oxygen, leading to anemia and fatigue. Mild thalassemia might not require treatment, and one can deal with it by taking steps to deal with symptoms like fatigue. Severe thalassemia needs proper treatment.

Types of Thalassemia

There are two types of thalassemia based on the chains of the hemoglobin molecule affected by the mutation of genes. If the alpha chain, made up of four genes, is affected, it is known as alpha-thalassemia, and in case the beta chain, made up of two genes, is affected, it is called beta-thalassemia. Alpha-thalassemia can arise from either one, two, or three mutated genes in the alpha hemoglobin chain. Beta-thalassemia is of two types, major (two-gene mutation of the beta hemoglobin chain) and minor (one-gene mutation of the beta hemoglobin chain) thalassemia, depending on the severity and symptoms of the problem.

Symptoms

Thalassemia symptoms in kids start developing only after six months of their birth because that is when the fetal hemoglobin replaces the normal hemoglobin. Following are the early symptoms of thalassemia:

  1. Weakness and frequent fatigue
  2. Jaundice, paleness of skin and yellowing of eyes
  3. Headache, chest pain,
  4. Slow growth and bone deformities
  5. Lack of appetite
  6. Muscle cramps
  7. Cold hands and feet
  8. Breathlessness and nausea
  9. Frequent infections due to weak immunity
Diagnosis

In children, thalassemia symptoms appear by the time they turn two years old. The identification of the carriers of thalassemia happens when their children get diagnosed with thalassemia. Doctors evaluate the following elements of the blood during a blood test for diagnosing thalassemia:

  1. Complete Blood Count (CBC), to check the level of RBCs and hemoglobin in the blood
  2. Reticulocyte Count, or the speed with which the bone marrow is producing the RBCs
  3. Iron test that helps to diagnose the causes of anemia

In addition to these, various types of genetic tests and prenatal tests help in the determination of the exact genetic disorder and whether a fetus has thalassemia or not, respectively.

Treatment

Blood transfusion: One of the most common and regulated treatments for thalassemia is blood transfusion. The process replenishes the lower levels of hemoglobin in the body by increasing the count of red blood cells in the blood. This process takes time, and the patient has to undergo eight to twelve transfusions at a regular interval in a year to complete the treatment. Many thalassemic patients can lead a healthy life with this treatment.

Bone marrow transplant: The function of bone marrow is to produce the blood cells, including White Blood Cells (WBCs), Red Blood Cells (RBCs), and platelets. A bone marrow transplant is efficient and helpful in the production of an appropriate amount of RBCs to maintain the level of hemoglobin in the body.

Iron Chelation: Regular and frequent blood transfusions can cause an excess of iron in the blood, which directly affects the heart and other vital organs of the body. Doctors prescribe deferoxamine or other drugs to remove excess iron and regulate the quantity of iron in the body.

Others: In the case of bone abnormalities or spleen enlargements, doctors may prescribe surgical procedures. Researchers and doctors are also working on other treatments like Gene Therapy.

Factors affecting cost of treatments in the states of India.

Thalassemia Treatment In Kolkata: Many patients get their treatment from the best hospitals in Kolkata as they offer excellent follow-up care as well.

Thalassemia Treatment In Pune: The cost of diagnosis and testing has been significant;y brought down in Pune due to an increase in the number of labs and hospitals.

Thalassemia Treatment In Delhi: Some of the best research institutes and hospitals in India are there in Delhi for the treatment of thalassemia.

Thalassemia Treatment In Mumbai: In addition to world-class infrastructure, Mumbai has some of the best surgeons and doctors with years of experience in treating thalassemia.

Testimonials

I took my baby girl Aaisha for the treatment of major thalassemia in 2018, and now she is completely healthy. It took a period of 8 months of regular blood transfusions, but thanks to Hospals, we could complete it without any issues.

- Himaya Sabib, Kenya

Blood transfusion is one of the costliest procedures for the treatment of thalassemia, and I wasn’t sure whether I would be able to afford it for my daughter or not. If it weren’t for the thalassemia treatment packages in India from Hospals, I would not have been able to provide the treatment to my daughter .

- Abebi. Nigeria

I had no idea I would be a carrier of thalassemia for my eight months old son. He completed his treatment in BLK Hospital of Delhi with a lot of help from Hospals.The credit of the successful treatment goes entirely to the doctors and staff of BLK and Hospals who took care of everything, including the follow-ups.

- Sarah Khan, Oman

My friend suggested me to get my son treated for his thalassemia in India through Hospals. To have someone like Hospals when you are traveling for any medical procedure is a blessing. The support I had for every minor detail from the staff was terrific, and I appreciate their detailed work.

- Eisa Fareed, UAE

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FAQs

Thalassemia is a genetic disorder, and family history is the most crucial factor that increases the risk of thalassemia. In the case of a family history of thalassemia, the chances of the parents passing a mutated hemoglobin gene are higher. Also, it is more common for people from specific ancestries. African, Americans or people from Southeast Asia are at a higher risk of thalassemia.
People suffering from thalassemia are at a higher risk of infections, heart diseases, and bone deformations. In addition to that, they are also at a higher risk of overload of iron deposits in the body. This is due to frequent blood transfusions. The spleen is also affected and may get enlarged due to a lack of RBCs in the body.
In thalassemia minor, a person gets one mutated gene in the beta hemoglobin chain. It happens if only one parent is thalassemic. Someone with thalassemia minor may or may not show all symptoms of thalassemia but can be a carrier of the disease.
In case a person is diagnosed with mild thalassemia and is facing symptoms like fatigue, they can deal with it by maintaining a healthy lifestyle. A healthy lifestyle comprises regular exercise and a nutritious diet. The person should also avoid the risk of infections by maintaining a healthy living environment.

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