Is thalassemia any harm to adults

First of all, you should go for further examination, suspected thalassemia does not mean confirmed thalassemia.

You should be clear about the type and extent of thalassaemia.

If you are diagnosed with thalassemia, your wife will also need further testing.

In general, there is a certain rate of missed detection of thalassemia, especially mild and static thalassemia.

Because you are an adult, thalassemia is most likely mild (although moderate thalassemia is not ruled out).

It doesn't affect you personally, but it's 50% likely to be passed on to future generations if it's mild.

If your wife is completely normal and the child is mildly thalassemia at best, it is not a big problem.

However, if your wife is also a thalassemia patient, your children may suffer from moderate to severe thalassemia.

Hello, if the couple is a carrier of homothalassaemia, each time you get pregnant, your child has a 1 4 chance of being.

Normal, 1 2 chances are carriers, and the other 1 4 chances are patients with thalassemia major, therefore, in heredity.

This is a very important condition in terms of counseling and prenatal diagnosis, and it is necessary to have enough mental accuracy to have a child.

It is important to pay attention to prenatal diagnosis and counseling, and miracles may occur, that is, to have a healthy and alive child.

sub, but only 25% of the time.

If one of the children is thalassaemia, 50% of the children are normal.

Thalassemia is caused by an imbalance in hemoglobin synthesis or may be due to a defect in the synthesis of one or more globin polypeptide chains. It can also be influenced by genetic factors. Thalassemia can cause anemia in the body and produce complications of other organs that affect the health of patients, causing anemia in the body, producing anemia symptoms, fatigue, dizziness, dizziness, memory loss, and numbness of limbs

Thalassemia is an inherited hemoglobinopathy that causes a deficiency because of an imbalance in hemoglobin, which causes thalassemia. Weakness, dizziness, memory loss, numbness of limbs, severe tissue necrosis shock or dysplasia, if there is a long-term thalassemia condition, it will also produce developmental disorders, thyroid function will also be very low, and it will also cause heart failure and death.

It may be because the usual diet and rest are completely irregular, it may be because of depression, it may be due to the influence of genetic factors, or it may be because of poor physical fitness; These people can experience tinnitus or dizziness, as well as cardiovascular disease, which can cause heart disease.

(1) Severe: Anemia, progressive aggravation of hepatosplenomegaly, jaundice, and dysplasia appear within a few days of birth, and its special manifestations are: large head, widening of the eye distance, saddle nose, forehead protrusion, cheek protrusion, its typical manifestation is a buttock-like head, long bones can be fractured.

Skeletal changes are caused by hyperhematopoiesis of the bone marrow, widening of the bone marrow cavity, and thinning of the cortex. A small number of patients develop a thoracic mass between the ribs and spine, and gallstones and leg ulcers may also be seen. Common complications include acute pericarditis, secondary hypersplenism, and secondary hemochromatosis.

2) Intermediate: mild to moderate anemia, most patients can survive to adulthood.

3) Mild: mild anemia or asymptomatic, generally found during the investigation of family history.

There are many people around me who have thalassemia, I also have it, but I don't feel uncomfortable, usually eat and sleep well, the spirit is still good, don't think about what harm it is, how many people in our ancestors have thalassemia, not the same can live a normal life, some hospital doctors in order to pit money, call us who have thalassemia to check or something, since this is a hereditary disease, it is impossible to cure, what is the use of checking, it is better to eat more nutritious, blood-replenishing food, exercise more. In short, I don't think it's any different from normal people.

Hello! Please don't worry too much, you have no symptoms, and you have recently donated blood to qualify, indicating that the so-called "thalassemia" detected in your marriage examination should be a thalassemia gene carrier, which has no impact on your health. However, if your subject happens to be a carrier of the same type of thalassemia (both are gene carriers, or both are gene carriers), there is a 1 4 (or 25%) chance of developing moderate to moderate or major thalassemia in the future, and such children will need frequent blood transfusions and iron removal agents, which will put a great burden on the family.

It is recommended that you do thalassemia gene testing first, and after determining which gene carrier it is, your subject should also be tested for the same thalassemia gene, if only you have it, and the subject does not, it doesn't matter. If both partners carry the same gene, by the third month of pregnancy, prenatal diagnosis should be done, and the fetus will have an abortion if it is moderate or major thalassemia.

In addition, to add that your parents do not have thalassemia, it only means that they are also thalassemia gene carriers, have no symptoms, and have not been to the hospital for check-ups, so they do not know.