How much does Thalassemia cost?

How much does Thalassemia cost?

Your cost treatment would be starting @ 22000 USD and extends up to 25000 USD.

Does thalassemia shorten your life?

A person with the thalassemia trait has a normal life expectancy. However, heart complications arising from beta thalassemia major can make this condition fatal before the age of 30 years.

Is Vitamin E Good for thalassemia?

One study conducted on beta-thalassemia intermedia patients indicated that vitamin E supplementation improved balance of the antioxidant system and inhibited the process of lipid peroxidation in patients[10].

Is there any permanent treatment for thalassemia?

The most common treatment for severe cases is regular blood transfusions to relieve the symptoms, which continue for life and have side-effects. The only cure currently available for thalassemia is a bone marrow transplant, which is only possible for a small proportion of patients.

Which test is done for thalassemia?

Doctors diagnose thalassemias using blood tests, including a complete blood count (CBC) and special hemoglobin tests. A CBC measures the amount of hemoglobin and the different kinds of blood cells, such as red blood cells, in a sample of blood.

Is there any treatment of thalassemia?

Mild forms of thalassemia trait don’t need treatment. For moderate to severe thalassemia, treatments might include: Frequent blood transfusions. More severe forms of thalassemia often require frequent blood transfusions, possibly every few weeks.

Which one is correct about thalassemia treatment?

A stem cell transplant is the only treatment that can cure thalassemia. But only a small number of people who have severe thalassemias are able to find a good donor match and have the risky procedure. For more information, go to the Health Topics Blood and Marrow Stem Cell Transplant article.

Why is HBE beta thalassemia so common in Asia?

As discussed by Williams and Weatherall (2012), HbE occurs at an extremely high frequency in many countries in Asia. Because there is also a high frequency of different β-thalassemia alleles in these populations, the coinheritance of HbE and β thalassemia, HbE β thalassemia, occurs very frequently.

What are the severest conditions of thalassemia?

The severest conditions are found in individuals with Hb E and β o -thalassemia, who usually have about 50–70% Hb F, the remainder being Hb E. Hemoglobin levels may be as low as 4–5 g/dl, and the clinical management of these patients is similar to that for those with thalassemia major.

What is the prevalence of thalassaemia in Thailand?

In some areas, it has replaced β-thalassaemia as the most common thalassaemia disorder. The frequency of HbE reaches 60% in many regions of Thailand, Laos and Cambodia with estimates of at least 100 000 new cases of HbE β-thalassaemia expected in the next few decades in Thailand alone.

Does HBE cause any clinical problems?

Although HbE alone does not cause any significant clinical problems, its interactions with various forms of α and β thalassemia produce a very wide range of clinical syndromes of varying severity. The molecular basis for the different forms of α and β thalassemia, which are coinherited with HbE, are described by Thein (2012)and Higgs (2012).