am 13 weeks pregnant and have had severe morning sickness since week 11. Doctor, what are the blood test results for anemia during pregnancy? I hope you can help me answer this question. Thank you.

Thalassemia (also known as congenital hemolytic disease) has been causing serious consequences to the race, and is a burden on the lives of patients and their families.

To best prepare before giving birth, mothers should get vaccinated with the vaccines recommended by doctors to help mothers and babies avoid dangerous infectious diseases such as measles, chickenpox, rubella, flu, hepatitis B, etc.

When performing an invasive prenatal diagnostic technique called chorionic villus biopsy, a sample of chorionic villus cells is taken for testing. Abnormal chorionic villus cells mean that the fetus is also abnormal.

Performing postnatal screening 24-72 hours after birth by taking blood from the baby's heel helps doctors screen for certain genetic diseases and metabolic disorders in children, reducing the number of children with physical and mental retardation and many other diseases.

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 in children causes hemolytic anemia, which is considered a burden on the family and community, causing serious consequences for the race. Treating hemolytic anemia requires a lot of effort, time and compliance from the patient.

Heel blood sampling is part of the newborn screening program for babies to detect early endocrine diseases and metabolic disorders that affect the health and physical and mental development of children. Especially dangerous diseases that are difficult to detect clinically at birth.

Thalassemia or hemolytic anemia is a disease that is passed from parents to children through a recessive genetic mechanism. A baby is born with the disease only if both the father and mother carry the disease gene. Currently, there are very simple hemolytic anemia tests that help determine the possibility of carrying the disease.

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.