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What is Thalassemia?

Thalassemia is a genetic blood disorder that affects the production of hemoglobin, a protein in red blood cells that carries oxygen to the body's tissues. It can cause anemia, fatigue, jaundice, and other complications.

How is Thalassemia treated?

The treatment for thalassemia depends on the type and severity of the condition. Treatment options include:

Blood transfusions: Regular blood transfusions can provide healthy red blood cells and improve symptoms.

Iron chelation therapy: Blood transfusions can lead to iron overload in the body, which can cause organ damage. Iron chelation therapy involves taking medication to remove excess iron from the body.

What is the cost of Thalassemia treatment?

The cost of thalassemia treatment can vary depending on the type of treatment required, the severity of the condition, and the location of the hospital. 

USD 19800 TO 24200

Who is the right doctor to consult for Thalassemia treatment?

A hematologist or a pediatric hematologist-oncologist is the right doctor to consult for thalassemia treatment.

What technology is used during Thalassemia treatment?

Blood transfusions and iron chelation therapy do not require any specific technology. Bone marrow transplant involves using advanced technology to match the patient with a suitable donor and to ensure a successful transplant.

What precautions should be taken during Thalassemia treatment?

It is important to follow the doctor's instructions for any treatment and attend all appointments. Patients undergoing blood transfusions should ensure that they receive blood from a reliable source to avoid infections. It is also important to maintain a healthy diet and exercise regularly to support overall health.

What are the key tests during Thalassemia treatment?

Regular blood tests will be conducted to monitor the patient's hemoglobin levels, iron levels, and overall health. Bone marrow transplant candidates will undergo a thorough evaluation to determine if they are eligible for the procedure.

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Frequently Asked Questions

Yes, congenital heart disease can be passed down from a parent to a child. If one or both parents have a congenital heart defect, there is an increased risk of their child having the condition as well. However, it is important to note that not all congenital heart defects are inherited and some can occur due to other factors such as infections during pregnancy or exposure to certain medications or substances.

The initial treatment process for a child with congenital heart disorder depends on the type and severity of the condition. This could include medications for visible symptoms and monitoring with regular checkups.

The tests for congenital heart disorders do not always require hospitalization. Many of the tests can be performed on an outpatient basis, which means the patient can leave the hospital or clinic on the same day. However, some tests may require a short hospital stay, particularly if the patient is an infant or young child.

The treatment options for congenital heart disease may depend on the type and severity of the condition. These options may include medications or procedures like cardiac catheterization.