Ascorbin 1000 contains Ascorbic Acid (Vitamin C). Vitamin C is needed for collagen formation, tissue repair in the body and participates in many important metabolic processes in the body.

Thalassemia is a hereditary hemolytic anemia or congenital hemolytic anemia. The main symptom of the disease is anemia. Thalassemia causes serious complications and becomes a burden for families and society. However, the symptoms of the disease can be completely controlled with a reasonable thalassemia patient care regimen.

Thalassemia was discovered and studied in 1925. The disease causes many serious consequences to the race, the lives of patients and the community. Levels of hemolytic anemia

Many babies with hemolytic disease whose parents did not screen them for the disease before birth require blood transfusions and treatment for most of their lives. Some babies with the disease only live a few years.

Thalassemia is a hereditary hemolytic anemia or congenital hemolytic anemia. It is one of the most common genetic abnormalities in the world today.

In cases with abnormal spleen problems, early examination, diagnosis and treatment are needed to avoid the risk of spleen rupture that is life-threatening. Laparoscopic splenectomy is the method indicated for cases of hypersplenism, thrombocytopenia, hemolytic anemia, etc.

Types of anemia are often distinguished by their characteristics and causes. It can be iron deficiency anemia or low red blood cell anemia. To better understand the causes of anemia, please refer to the 4 common types of anemia below.

Anemia is a condition in which there is a lack of quality red blood cells to transport oxygen to the cells. When you have anemia, you will feel weak and tired. The cause of anemia in each person is different and can be temporary or long-term. So what causes anemia?