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Thalassemia Treatment Cost in Turkey
The body produces less healthy red blood cells and hemoglobin as a result of thalassemia, a genetic blood disorder (an iron-rich protein in red blood cells). The two most common types of thalassemia are alpha and beta-thalassemia. The most severe form of thalassemia is referred to as “alpha thalassemia major” or “hydrops details.” The severe form of beta-thalassemia is referred to as “cooley’s anemia” or “thalassemia minor”. Thalassemia treatment in Turkey provides you with a comprehensive strategy as well as the appropriate medical facilities. Top medical vacation destinations such as Turkey are popular among patients from all over the world…
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    What Are the Types of Treatment Available in Turkey? Treatment of thalassemia in Turkey depends on the type and severity of the disorder. People who have alpha or beta thalassemia or who are carriers need little or no treatment. Here are some standard treatments that are used to treat moderate…
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    The Most Important Frequently Asked Questions

    Q: What Is the Most Effective Treatment for Thalassemia?

    A: Stem cell or bone marrow transplants are the only cure for thalassemia, but they are rarely used due to the high risks involved. Stem cells, which can develop into various types of blood cells, are produced in bone marrow, the spongy tissue found in the centre of some bones.

    Q: Is It Possible to Treat Thalassemia?

    A: Mild cases of thalassemia trait do not require treatment. Treatments for moderate to severe thalassemia may include: Regular blood transfusions More severe forms of thalassemia frequently necessitate blood transfusions, sometimes every few weeks.

    Q: Can You Lead a Normal Life If You Have Thalassemia?

    A: Individuals with thalassemia major can enjoy a near-normal lifestyle and regular physical and emotional development from childhood to adulthood, including parenthood, if the disease is fully compensated by ideal treatment.

    Q: What Causes People to Develop Thalassemia?

    A: Thalassemia is caused by DNA mutations in cells that produce haemoglobin, the substance in red blood cells that transports oxygen throughout your body. The mutations that cause thalassemia are passed down from parents to children.

    Q: What Should Thalassemia Patients Eat?

    A: Individuals are encouraged to eat a balanced diet consisting of protein, grains, fruits, and vegetables, and they may need to pay special attention to avoid consuming excessive amounts of iron.

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