Category: BMT/Thalassemia

  Access to affordable and quality healthcare services remains a significant challenge in many developing countries, especially when it comes to advanced medical treatments like bone marrow transplants. However, in recent years, India has emerged as a leading destination for free bone marrow transplants, offering hope to patients from Africa and Bangladesh who seek life-saving…

Yes, thalassemia is typically associated with a microcytic hypochromic type of anemia. Microcytic refers to abnormally small red blood cells, and hypochromic refers to red blood cells with reduced hemoglobin content. In thalassemia, the genetic mutations affect the production of globin chains, which are essential components of hemoglobin. As a result, the production of normal…

Reading a thalassemia test report may require some understanding of the terminology and values provided. Here are some key components to consider when interpreting a thalassemia test report: 1. Hemoglobin levels: The test report may indicate the levels of hemoglobin in the blood. Normal hemoglobin levels vary depending on age and gender. Lower hemoglobin levels…

A balanced and nutritious diet is important for individuals with thalassemia to support overall health and manage the condition effectively. While there is no specific diet to cure thalassemia, certain foods can provide essential nutrients that support red blood cell production and help maintain optimal health. Here are some food recommendations for individuals with thalassemia:…

No, thalassemia is not a sexually transmitted disease. Thalassemia is an inherited blood disorder caused by genetic mutations in the genes responsible for producing hemoglobin. It is passed down from parents to their children through the transmission of these mutated genes. Thalassemia is not transmitted through sexual contact or any form of intimate activity. The…

Hemoglobin E beta thalassemia (HbE β-thalassemia) is a genetic condition that occurs when a person carries both the hemoglobin E mutation and a beta thalassemia mutation. The severity of HbE β-thalassemia can vary widely, ranging from mild to severe, depending on the specific genetic mutations involved. In general, HbE β-thalassemia is considered a moderate to…

Testing for thalassemia typically involves a combination of blood tests and genetic analysis. Here are the common methods used to diagnose thalassemia: 1. Complete Blood Count (CBC): A CBC is a routine blood test that measures the number and characteristics of red blood cells, white blood cells, and platelets. Thalassemia can be suspected if the…

Yes, thalassemia can occur in adults. Thalassemia is typically an inherited condition that is present from birth. However, the symptoms of thalassemia may not manifest until later in childhood or even adulthood, depending on the severity of the condition. In some cases, individuals with mild forms of thalassemia may not experience significant symptoms until later…

No, thalassemia is not a form of blood cancer. Thalassemia is an inherited blood disorder characterized by abnormal hemoglobin production, which leads to a reduction in red blood cells and oxygen-carrying capacity. It is caused by genetic mutations that affect the production of hemoglobin. Blood cancer, on the other hand, refers to a group of…