WebBeta-thalassemia. Two genes are involved in making the beta hemoglobin chain. You get one from each of your parents. If you inherit: One mutated gene, you'll have mild signs … WebBeta thalassemia affects the hemoglobin in the red blood cells. All red blood cells contain hemoglobin, which carries oxygen from the lungs to all parts of the body. People with beta thalassemia do not make enough hemoglobin. People with beta thalassemia trait have both normal hemoglobin A and the abnormal beta thalassemia (β) hemoglobin in ...

Beta Thalassemia Article - StatPearls

WebThalassemias. Thalassemia is an inherited blood disorder that affects your body’s ability to produce hemoglobin and healthy red blood cells. Types include alpha and beta … dailymotion love is in the air capitulo 154

Types of Beta Thalassemia - WebMD

WebMay 8, 2024 · Beta-thalassemia is an inherited disorder resulting from various mutations (over 200 disease-causing mutations have been identified) or, rarely, deletions of the beta-globin gene (HbB) on chromosome 11. ... The reported carrier prevalence in Greek and Turkish populations in Cyprus is up to 15%. The beta form of thalassemia is particularly prevalent among the Mediterranean peoples and this geographical association is responsible for its naming: thalassa (θάλασσα) is the Greek word for sea and haima (αἷμα) is the Greek word for blood. In Europe, the highest concentrations of the disease are found in Greece and the Turkish coastal regions. The major Mediterranean islands (except the Balearics) such as Sicily, Sardinia, Corsica, Cyprus, Malta and Crete are heavily affecte… WebApr 17, 2002 · Sickle/beta-thalassemia is the most common sickle syndrome seen in people of Mediterranean descent (Italian, Greek, Turkish). Beta-thalassemia is quite common in this region, and the sickle cell gene occurs in some sections of these countries. ... The combination of hemoglobin E and beta-thalassemia produces a condition more … biology courses wvu