Thalassemia is a genetic disorder, with no treatment options other than blood transfusions and bone marrow transplants. Mild symptoms can be relieved through diet, nutritional supplementation, and artificial blood substitutes. Severe symptoms require blood transfusion treatment. If one parent has thalassemia, the child has a 20% chance of inheriting the disease. It is recommended to seek treatment at a regular, professional hospital.
Thalassemia is a group of hereditary hemolytic anemia caused by defects in the globin gene, leading to changes in the composition of hemoglobin. This article introduces the treatment methods for thalassemia and dietary recommendations for children.
Explore the different types of thalassemia and the interpretation of genetic testing results, providing professional medical insights.
A 9-year-old child suddenly experiences headaches and jaundice, with yellowish skin and lack of color. They also have nausea and palpitations. After hospital checks, no specific cause is found. The doctor suspects thalassemia. If both parents do not have a family history of thalassemia, what is the likelihood of the child being affected?
HbH Disease is a type of thalassemia that may require bone marrow transplantation for treatment.
Explore the definition, treatment methods, and the importance of genetic testing for HbH disease.
What should SEA deficient alpha thalassemia patients pay attention to in their daily life and diet?
Understand the different types of thalassemia, including severe, intermediate, and mild forms, along with their characteristics and impacts.
Neonatal disease screening for HBA abnormalities typically refers to thalassemia, which may be accompanied by clinical manifestations or merely a temporary elevation. Early treatment and consideration of genetic factors are recommended.
