About Thalassemia

Alpha-Thalassemia, also known as alpha thalassemia, is related to hemoglobin h disease and alpha thalassemia-intellectual disability syndrome type 1, and has symptoms including angina pectoris, chest pain and edema. An important gene associated with Alpha-Thalassemia is HBA2 (Hemoglobin Subunit Alpha 2), and among its related pathways/superpathways are Glucose / Energy Metabolism and Binding and Uptake of Ligands by Scavenger Receptors. The drugs Metformin and Peginterferon alfa-2b have been mentioned in the context of this disorder. Affiliated tissues include bone, spleen and liver, and related phenotypes are microcytic anemia and abnormal hemoglobin

Major Symptoms of Thalassemia

Thalassemia is a genetic blood disorder that affects the production of hemoglobin, which is responsible for carrying oxygen in the blood. The major symptoms of thalassemia include anemia, fatigue, weakness, shortness of breath, and anemia.

Suitable Lifestyle for People with Thalassemia

Thalassemia is a hereditary blood disease that usually causes anemia, splenomegaly, jaundice and other symptoms. Therefore, patients need to pay special attention to maintaining a healthy lifestyle to help relieve symptoms and prevent complications. First, patients need to maintain adequate rest and sleep time to avoid overexertion and fatigue. Secondly, you need to pay attention to a balanced diet, eat more foods rich in iron, vitamin B12, folic acid and other nutrients, and avoid eating foods that are too greasy, spicy, and irritating. In addition, patients also need to maintain a good attitude and avoid mood swings and excessive stress to help improve blood circulation and reduce symptoms. In conclusion, for patients with Thalassemia, lifestyle adjustments are important to relieve symptoms and prevent complications. It is recommended that patients develop a reasonable lifestyle under the guidance of a doctor and strictly implement it.

Other Diseases

Beta Thalassemia Alpha-Thalassemia Myelodysplasia Syndrome

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