Thalassemia

summary

Due to gene mutation, hemoglobin globin chain formation disorder, known as thalassemia. The clinical manifestations of different types of thalassemia vary greatly. The most severe cases may die before the birth of the fetus, and the least severe cases may be asymptomatic without anemia for life. Most of this disease occurs in infants, manifested as anemia, weakness, abdominal caking, retardation and so on. So can this disease be inherited? How can we find this kind of symptom?

Thalassemia

Pay attention to rest and nutrition, and actively prevent infection. Supplement folic acid and vitamin E appropriately. Avoid strenuous activities and heavy physical labor, and stay in bed when severe anemia occurs.

Paying attention to mental health is of great significance to the prevention of deficiency of labor and blood. It is not only the cause of disease, but also can aggravate the process. Therefore, patients with this disease should keep a happy and optimistic mood.

Pay attention to diet, should eat nutritious food, where spicy flavor, too greasy, cold unclean things, when fasting or less food. Due to the physiological characteristics of children's spleen and kidney often insufficient, feeding should be reasonable, in order to avoid hunger and satiety impermanence, partiality, unclean diet damage children's spleen and stomach.

matters needing attention

The appearance and growth of thalassemia patients are the same as those of normal people. Vitamin supplement is the same as that of ordinary people. Because it is difficult to detect the disease, iron is often given to supplement blood. Premarital examination, marriage object should test whether thalassemia with cause, if so, pay special attention to prenatal examination.