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 seeking treatment and high-quality medical care. In Turkey, thalassemia patients are treated with chelation therapy, stem cell transplants, and routine blood transfusions.

In comparison to the cost of the identical operation in nations like the United States, United Kingdom, Germany, and others, the cost of thalassemia treatment in Turkey is much lower.

What Does Thalassemia Means?

Thalassemia is a genetic medical condition in which the body produces less hemoglobin than normal. Hemoglobin is found in red blood cells and aids in the transport of oxygen. This blood disorder can cause anemia and make the patient tired all of the time. People with mild thalassemia may not require treatment, but those with more severe forms may require regular blood transfusions or a bone marrow transplantation. The medical team assists the patient in managing fatigue by recommending a healthy diet, regular exercise, and other similar measures.

What Are the Signs and Symptoms of Thalassemia?

Thalassemia signs and symptoms are typically determined by the type and severity of the patient’s condition. Some common signs and symptoms of Thalassemia include:

• Fatigue
• Weakness
• Pale or yellowish skin
• Facial bone deformities
• Slow growth
• Abdominal swelling
• Dark urine

Read More – Thalassemia Treatment Cost In India

What Are the Types of Thalassemia?

One of two things can be meant when discussing distinct “types” of thalassemia: either the precise region of hemoglobin that is afflicted (typically “alpha” or “beta”) or the severity of thalassemia, which is denoted by terms like “trait,” “carrier,” “intermedia,” or “major.” Alpha and beta are the names of the two distinct components that make up hemoglobin, which delivers oxygen to all of the body’s cells. The term “alpha” or “beta” used to describe thalassemia refers to the portion of hemoglobin that isn’t produced. There are not enough constituent parts to produce normal amounts of hemoglobin if either the alpha or beta portion is not produced. Alpha thalassemia is low alpha. Beta thalassemia is referred to as low beta. 

The terms “alpha thalassemia” and “beta-thalassemia,” which are called after flaws in these chains, refer to two different kinds of thalassemia:

1. Alpha-thalassemia

The production of the alpha hemoglobin chain involves four genes. Your parents give you two each. Upon inheriting:

• One mutated gene: You won’t show any symptoms of thalassemia if one gene is altered. However, because you have the illness, you run the risk of passing it to your offspring.

• Two mutated genes: You will have modest thalassemia symptoms because you only have two faulty genes. We could refer to this situation as an alpha-thalassemia phenotype.

• Three mutated genes: Your indications and symptoms will range from mild to severe due to three faulty genes.

2. Beta-thalassemia

The beta-hemoglobin chain is produced by two genes. Your parents each give you one. Upon inheriting:

• One mutated gene: You’ll have minor symptoms and indicators if one gene is altered. Thalassemia minor, also known as beta-thalassemia, is this condition.

• Two mutated genes: Your indications and symptoms will range from mild to severe due to two faulty genes. Thalassemia major, often known as Cooley anemia, is the name of this illness.

The majority of newborns with two faulty beta hemoglobin genes are normal at birth, but within the first two years of life, signs, and symptoms start to appear. Two faulty genes can also cause thalassemia intermedia, a lesser type.

Why Turkey Is a Top Destination for Thalassemia Treatment?

Turkey, which is frequently referred to be a Eurasian nation, is located on the border of Asia and Europe. Turkey’s culture is a distinctive tapestry that combines both eastern and western aspects, and this is furthered by its rich history as the great Ottoman Empire’s successor state.  Turkey is categorized as a regional power as well as a developed nation much like the United States and Western Europe. And one of the top 10 locations worldwide for medical tourism. 

Turkey is a popular choice for medical tourism for several reasons, including;

• Accredited hospitals with modern equipment
• Superior health care services
• Affordable rates
• Service and culture
• Geographical place
• Traditional, historical, natural, and tourism destinations

Three significant benefits of visiting Turkey for medical treatment are the low cost, the excellent standard of care, and the quick access to top-notch care. Turkey’s main advantage over other nations is the substantial discounts it offers. The cost of several procedures is 50% to 70% less than it would be in the EU. Turkey is conveniently situated, only two to three hours by flight from the Middle East and Europe’s largest cities. More than 70 nations offer visa-free entry to Turkey.

Know More – Medical Tourism in Turkey