What happens to a child born of severe thalaemia on both sides?

The child born from both parties is also severe thalassemia, and then the child will have anemia in the first few days of birth, hepatosplenomegaly, progressive aggravation of jaundice and dysplasia, and its special manifestations are: large head, widening of the eye distance, saddle nose, forehead protrusion, cheek protrusion, and its typical manifestations are buttock-like heads, and long bones can be fractured. Skeletal changes are caused by hyperhematopoiesis of the bone marrow, widening of the bone marrow, 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. Most people with thalassemia who receive a perfect ** throughout their lives are able to grow normally during puberty and have normal sexual development.

It is possible to adopt or do IVF to get a child. You can consult the test tube on the self-service platform of Yiyu, and now there is still the March 8th Goddess Day event, the more people who join the group, the more discounts will be for the event, and there will be air tickets at the same time.

The child's thalassemia will be more severe. For example, two carriers will give birth to a severe thalassemia. The two thalassemia were born heavier and are estimated to not survive.

This kind of pregnancy is a high-risk event, and I am afraid that I will bleed at that time. It is also possible for children to be inherited, so it is recommended to adopt one. Children are also pro when they are raised from an early age, as the saying goes, it is better to raise grace than to raise grace, you still take care of yourself!

<> thalassemia is an inherited disorder in which the hemoglobin in a person's body is poorly broken down, leading to anemia and other serious physical problems. For people with thalassemia, the risk of fertility is higher because their children may also be affected by the disease. If two people with thalassemia have children, there is a high chance that the child will have thalassemia.

If a person with thalassemia is born to a normal person, the child will become a carrier of thalassemia, but not necessarily the disease. Therefore, if you or your partner has thalassemia, you should consult with your doctor to assess the risks and consider appropriate contraception or other options before considering having children.

Thalassemia, also known as sickle cell anemia, is an inherited disorder that carries some risks for women with thalassemia in both pregnancy and childbirth. People with thalassemia don't have hemoglobin that doesn't transport oxygen properly, which can lead to anemia and a number of other health problems. At the same time, patients may also have some reproductive health problems, including fertility disorders and infertility.

However, for some people with non-specific thalassemia, pregnancy and childbirth are possible. However, this process requires close monitoring and some necessary measures to ensure the health of both mother and child. Therefore, if you suffer from thalassemia and intend to become pregnant, it is advisable to consult a medical professional.

<> thalassemia is a genetic disorder in which people lack a protein called hemoglobin in their red blood cells, leading to symptoms such as anemia. People with thalassemia can have children, but there may be some risks and challenges during pregnancy and childbirth. Factors such as the patient's age, physical condition, and the type and severity of thalassemia are considered.

Patients with thalassemia are advised to consult their doctor before giving birth and to receive comprehensive genetic counseling and testing.

<> I'll use the examples around me to ask the subject's question. My friend is currently more than four months pregnant and has been diagnosed with thalassemia. Doctors advise against keeping children.

The child born will also have a good chance of inheriting the disease. If you want to have a baby, you have to do IVF. The cost is around 100,000, but the success rate is only 50%.

Thalassemia is a disease with a low rate. It is a disease caused by congenital chromosomal abnormalities. Because thalassemia is a genetic disease, the biggest concern is that the disease will be passed on to the child because thalassemia is caused by a genetic defect.

If both spouses are carriers, consider carefully whether to have children, as children may inherit thalassemia. The child born must have thalassemia and present with moderate and severe anemia. Blood tests should be done before pregnancy.

In terms of peptide chain detection and genetic analysis distribution, two patients with homothalassemia will have a chance to give birth to patients with severe anemia.

Doctors recommend a personal birth check-up. Today's medicine also has a chance to give birth to normal children. Thalassemia is a congenital genetic disorder.

If both spouses have thalassemia. Although it does not affect fertility, the remaining children are likely to inherit the disease. Whether or not a person with thalassemia can have children cannot be generalized.

Patients should bring all their test results to an experienced doctor to see if they can have children. Thalassemia is divided into types and types, thalassemia major patients are prone to spontaneous abortion in the second trimester, and it is difficult for thalassemia major children to be born during routine examinations. Most patients survive only on blood transfusions.

Some patients may be able to achieve long-term stable status through bone marrow transplantation. However, due to the different opportunities for thalassemia major in different patients, some thalassemia carriers can have children, while some patients may develop thalassemia major after childbirth.

Patients with thalassemia mild can have children, the disease does not pose a major threat to the body in the mild stage, and as long as the spouse is normal, the child is generally healthy. However, during pregnancy, patients should take more rest, ensure nutritional intake, and also pay attention to monitoring the genetic status of the child.

Thalassemia is a genetic disease, mainly distributed in Mediterranean countries and Asia, and Guangxi, Guangdong and Hainan in China are the areas with a high incidence of thalassemia.

It can be divided into four grades: very light, light, intermediate and heavy.

Normally, each person will have two sets of normal hemoglobin genes; One group came from the father and the other from the mother.

Thalassemia can occur if one or more abnormal genes are inherited from a parent. Thalassemia must be inherited from the parents, and it is not contagious.

Very thalassemia minor has no anemia, so it is also called thalassemia gene carrier, thalassemia minor only has mild anemia, which is mostly found during physical examination, and most patients with these two types will not know that they have this gene.

Intermediate patients with moderate anemia can be treated with drugs** and splenectomy to increase hemoglobin, but only to improve anemia, not **, and relatively heavy blood transfusion.

Thalassemia major is a very serious disease that develops 3-6 months after birth, and they require regular blood transfusions and iron removal for the rest of their lives**.

If both couples have the thalassemia gene, i.e. both have thalassemia minor, 25% of their children will have thalassemia major, 50% thalassemia minor (gene carrier), and 25% normal.

If only one parent is thalassemia minor or a gene carrier, 50% of their children are normal children, 25% are thalassemia minor (gene carriers), and there will be no thalassemia major children.

Be sure to have a premarital check-up, and it's best not to carry both.

After the child is born, it is necessary to be tested for thalassemia so that you know about it.

Hello, if you have thalassemia then it is possible to have the opportunity to pass it on to your children, it also depends on whether your husband has thalassaemia, if only one party has a small chance of thalassemia hereditary, if both parties are thalassemia then the probability of inheritance is very high.

If it is a patient with the same type of thalassemia, the children born to them are more likely to be diseased, so it is necessary to do a good job of genetic counseling, prenatal diagnosis and selective fertility from the perspective of eugenics and fertility in advance according to their own conditions.

Thalassemia is a group of genetic disorders that are classified as severe, moderate, mild, and very mild.

Patients with moderate thalassemia major, if they do not **, cannot live to adulthood.

Very light is only carried, and I don't get sick, but it's genetic.

If both spouses have it, the child will definitely have it, and it is likely to be medium to heavy.

If only one of the couple carries it, there will be no medium to heavy and it is possible to give birth to a light and carrier child.

Carriers, untested may not be known for life.

Therefore, both husband and wife should be tested before marriage, especially in high-incidence areas such as Liangguang and Fujian.

For the sake of themselves and their children, both husband and wife cannot have children if they have land poverty.

1.Thalassemia does not affect fertility, but it does affect the child's constitution and genetics.

2.In general, if two people with the same type of thalassemia are combined, there is a chance of giving birth to a person with severe anaemia. In order to effectively prevent the disease, blood needs to be drawn for peptide chain testing and genetic analysis, if it is confirmed that the child and the spouse belong to the same type of very mild or minor thalassemia, the child will have a 1 in 4 chance of being completely normal, 1 in 2 chance of becoming a mild anemia patient, and a 4 in 4 chance of becoming a moderate or severe anemia patient.

In view of the lack of the best methods for this disease and the poor prognosis of moderate and severe clinical cases, doctors should give medical advice to patients with a positive family history or prenatal genetic diagnosis in terms of marriage, and conduct premarital examination and prenatal genetic diagnosis of the fetus to avoid the occurrence of the next generation of children.

You should be cautious and listen to your doctor's advice.

Husband and wife have thalassemia, can also have children, mainly depends on the genotype of thalassemia of the husband and wife, if the husband and wife of the thalassemia genotype is different, then there is generally no effect, for example, one party is a thalassemia, the other party is thalassemia, then the husband and wife are different, the child born generally will not have severe anemia, and there is no need to do prenatal diagnosis, if the husband and wife are the same type of thalassemia, there is also a chance to give birth to a healthy child, but there is also a chance to form a fetus with severe thalassemia, so after each pregnancy, Prenatal diagnosis is required.

Thalassemia is a hereditary disease, and it is important to have a preconception test before having a child, and if both partners have this gene, there is a good chance of having a thalassemia child.

Ding Xiaoqing: Whether people with thalassemia can have children, this question is related to us because it is a hereditary disease, it is hereditary, if there is a next generation, its genes, ** to both parents, then if the mother is a thalassemia patient, it is recommended that he is if it is a father, it is best for him to have a child before he must do a preconception examination, if both parties have this gene, it is best to advise her not to, because she has a great chance of giving birth to a thalassemia child.

Hello sister, why do you need to make offerings too? Why do you need so many things to offer, they are all poor people, I have premature aging at the age of 20, and my husband also knew when I got married at that time, and I didn't want to hide it from him, which would be too unfair to him. Facts have also proved that my husband truly loves me.

I remember that I didn't get pregnant in the first year of marriage, and then in the second year, I kept going to the hospital to do IVF, and I tried to do it three times, each time I took two or three, and I didn't succeed after moving it four times, and now I can't imagine the feeling of collapse at that time.

At that time, the doctor directly sentenced him to death, saying that it was basically impossible to conceive for himselfRecommend Jinbei egg donation, it may be that I am young with a good endometrium, with four tubes, and a tube is removed, I feel that my luck is still very good, unconsciously said so much, now I am not very clear about the situation, sisters pay more attention not to be deceived, and finally wish you a good pregnancy as soon as possible, if you are satisfied, you will adopt it.

Yes, I also had thalassemia in the examination at that time, and there was nothing abnormal after the baby was born, and the baby was very healthy.

Thalassemia patients can also get pregnant, if they have thalassemia mild, they should be checked accordingly when they are pregnant, if their parents have thalassemia severe, the fetus may be stillborn or terminated, so they must do a good job of prenatal check-ups, and do regular check-ups.

Don't be afraid of a slight slight, I have a colleague who was pregnant and found a slight thalassaemia, and then the baby was born and it was nothing.

Because thalassemia is a genetic disease, the most worrying thing for patients is that such a condition will be passed on to children, it is generally believed that thalassemia is a hereditary disease, and it is not recommended for patients to have children, but if thalassemia patients carry different types of thalassemia genes, they can have children, so thalassemia can be fertile.

Thalassemia is caused by a genetic defect that can affect a child if one parent is a thalassemia carrier. The specific genetic probability is as follows: if a carrier of thalassemia minor marries a normal person, his offspring have a 50% chance of becoming a carrier of thalassemia mild.

Married to resting thalassemia and minor thalassaemia, there is a 1 4 chance of giving birth to a child with thalassemia. If the couple is a carrier of the same thalassemia gene, each pregnancy, the fetus has a 1 4 chance of being normal, 1 2 of the chance of being a gene carrier, and 1 4 of a 4 chance of being a thalassemia major patient, and if both husband and wife carry different thalassemia genes, or only one of them carries the thalassemia gene, the child will not have thalassemia.

However, pregnant women with thalassemia major should pay special attention, and if the fetus is confirmed to have thalassemia severity, it is best to perform artificial termination of pregnancy. If the test results show that the fetus is genetically normal or has mild thalassemia, the pregnancy can be safely continued. Mild thalassemia does not need special ** intermediate and severe thalassemia can take blood transfusion and iron removal **, pay attention to rest and nutrition in daily life, actively prevent infection, and appropriately supplement folic acid and vitamin E.