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Abnormal bone structure, especially in the face and skull. Heart problems. Iron overload. While some babies show signs of thalassemia at birth, others may develop symptoms during the first two years of … Thalassemia is a blood disorder in which the body makes an abnormal form of hemoglobin. Learn more about its symptoms and how it's diagnosed.

This is because neonates have a different type of hemoglobin, called fetal hemoglobin. Thalassemia can take on myriad forms, and depending on what you're dealing with – alpha thalassemia or beta thalassemia, thalassemia trait, or thalassemia major – your symptoms may vary. Watch for signs like stunted growth, delayed puberty, pale or jaundiced appearance, fatigue, bone development issues, and dark colored urine. Thalassemia: Symptoms and Risk Factors. Thalassemia is an inherited impairment of hemoglobin production.

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Symptoms will not show until the age of 6 months in most infants with beta thalassemia and some types of alpha thalassemia. This is because neonates have a different type of hemoglobin, called fetal hemoglobin.

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A more severe form of alpha thalassemia occurs in a condition known as hemoglobin Bart hydrops fetalis syndrome, which is also called Hb Bart syndrome or alpha thalassemia major. The milder form is called HbH disease. PDF | Key words: Ethnicity, Thalassemia zone, Social Stigma Background: Thalassemia, the autosomal recessive syndrome is the most common monogenic Thalassemia patients in West Bengal. 2018-07-17 · Unlike Thalassemia Major, Thalassemia Minor has only one defective beta globin gene A normal hemoglobin molecule is made up of two identical beta and two identical alpha chains. The defective beta chains are compensated by delta chains resulting in formation of hemoglobin A2. In the screening schedule thalassemia awarness programme was conducted in various rural areas of West Bengal. We mainly confronted with the Sardar tribes in extreme south of West Bengal.

Anemia can result in feeling tired and pale skin. There may also be bone problems, an enlarged spleen, yellowish skin, and dark urine.
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Bengal Cancer Thalassemia & Dengue Awareness Page. 347 likes · 1 talking about this. BCTDA - is a Social Welfare & Epidemic Awareness Page in Social Beta thalassemia causes variable anemia that can range from moderate to severe, depending in part on the exact genetic change underlying the disease. Beta thalassemia can be classified based on clinical symptoms. Beta thalassemia major usually causes severe anemia that can occur β-thalassemia Major People with β-thalassemia Major usually have no symptoms at birth, but signs and symptoms often appear between 6-24 months of age.

Carriers typically do not show signs or symptoms of the condition; although some carriers of beta thalassemia develop mild anemia.
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If you have one, your body makes fewer healthy red blood cells and less hemoglobin. Hemoglobin is a protein that carries oxygen to the body. That leads to anemia. Thalassemias occur most often among people of Through an ethnographic approach, privileging Bengali constructions of personhood, we have unraveled the process by which a medically desirable action becomes socially and culturally undesirable, thus complicating the prevention of thalassemia in Bengali society.

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Heart problems. Iron overload.