The thalassemias is a group of hereditary disorders with impaired production of functional hemoglobin. In this report we described a rare case of compound heterozygous mutation of South-East Asia type hereditary persistence of fetal hemoglobin (SEA-HPFH) and β -thalassemia that allowed prenatal diagnosis to be performed in a subsequent pregnancy in the family.

I am currently 20 weeks pregnant with twins. I have heterozygous alpha 3.7 deletion hemolytic anemia. Doctor, can you tell me if it is dangerous to have heterozygous alpha 3.7 deletion hemolytic anemia during pregnancy? My husband is probably normal because his blood formula is normal. I hope the doctor can advise me. Thank you.

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.

Deferiprone (trade name Ferriprox) is a medication used to treat iron overload in patients with thalassemia major. Ferriprox is often indicated when traditional chelation therapy is contraindicated or ineffective.

According to incomplete statistics, about 20% of Vietnamese children under 5 years old are iron deficient. While malnutrition, protein, and energy are of concern to the community, iron deficiency causing anemia has not received due attention. Iron deficiency or abuse of iron-containing drugs are both harmful and have negative consequences on children's health.

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.

Healthy women between the ages of 35 and 40 can still have safe pregnancies and give birth to healthy babies. However, genetic screening before and during pregnancy for pregnant women aged 35 and over has many benefits.

Hemolytic anemia is a genetic blood disorder that causes your body to have less hemoglobin than normal. So, in addition to treatment, what nutrition for people with hemolytic anemia will be like to increase the amount of hemoglobin in the body?

Thalassemia is a hereditary hemolytic anemia caused by a deficiency in the synthesis of one or more polypeptide chains in the globin of hemoglobin. The word thalassemia is a Greek word meaning sea blood disease, because it was first discovered and is common in the Mediterranean region. Depending on the deficiency in the alpha, beta or both delta and beta chains, it is called α-Thal, β-Thal or delta –β Thal.

Thalassemia is a chronic disease that requires lifelong monitoring and treatment, especially severe Thalassemia. Patients must have blood transfusions and iron excretion monthly, so compliance with treatment requires effort from the patient, family, and support from society.

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