After pregnancy, I found out that my husband s family has a genetic disease, will the child have a b

It is necessary to go to a regular hospital in time to see what the disease is, follow the doctor's advice, if it will be hereditary, it is necessary to terminate the pregnancy in time, and if it will not be inherited, you can raise the fetus with peace of mind.

After pregnancy, it is found that the husband's family has a genetic disease, it depends on what kind of genetic disease it is, since it is a genetic disease, most of them have an impact on the child, you should consult a doctor, if it doesn't work, you can't ask for it.

Genetic diseases must have an impact on the child, and it is necessary to go to the hospital to consult a doctor, who is more professional and can give you advice to see if the child wants or not.

It depends on what the genetic disease of your husband's family is, if it is diabetes or other chronic diseases, it may not have much impact on the child, but if it is a blood disease, the impact on the child is still relatively large.

If there is a hereditary disease in the family, if you have a child, the impact on the child is great, because he is likely to inherit the disease.

It may have an impact, but it is not necessarily, because there are heredity and variations in the genes of biology, some diseases can be inherited, some diseases will not be inherited, and some have to be divided into men and women, so it is best to listen to the doctor and don't worry about it.

If you are pregnant, the safest way is to do a genetic test, if it can be diagnosed among the known genetic diseases, then the child must not be wanted.

If the husband has a family genetic disease but wants to have a child, then he must take the initiative to ask the doctor and do a good job of relevant genetic disease tests after pregnancy, and terminate the pregnancy if there is a problem.

The birth of every child is not easy, when both parties want to have children but encounter a husband with a family genetic disease, we can choose to give up having our own children, or we can choose to "choose" our own children more uncomfortable.

1. If the husband's family genetic diseases are relatively mild, we can choose to actively check after pregnancy, eugenics and eugenics for family genetic diseases, in fact, we should know more when planning to have children, to find out whether these diseases can get pregnant.

If these family genetic diseases are actually common in life and do not affect the life of the child, we can rationally plan for pregnancy; During pregnancy and prenatal check-ups, we should ask the attending doctor and perform various genetic tests to ensure that the child grows up healthily as much as possible. If there is a more serious disease than the father because of the genes of both parties, we should "choose" ruthlessly, and do not let them be born who delays the family and harms the "future of the child".

2. If the husband has a serious family genetic disease, it is safe and it is not recommended to have children, which is very harmful to the family, and if the husband's family genetic disease is more serious, almost 100% of the offspring are inherited and have serious effects, it is not recommended to get pregnant at all.

may be looking forward to having your own child, but such a high-risk pregnancy is not recommended, and the delay is not only time, but also feelings; Constantly challenging high-risk genetic diseases and almost never having a child is a big shock for women and families, don't try to challenge the "strong wall", DNA mutation is not as easy as we expect. Therefore, families with special genetic diseases really do not want to have their own children, which has a great impact on the family.

The family needs to choose from the husband's genetic disease, and if you can have a child, you can try, and it is not recommended to get pregnant.

If your husband has a family genetic disease, it is recommended that you should go to the hospital for a check-up and listen to the doctor's professional advice, only in this way can you ensure the healthy growth of the child.

This depends on the severity of the genetic disease, if it is a particularly serious and painful genetic disease, it is recommended not to have children, if this genetic disease is not particularly serious, and there is a ** possibility, then you want to have one.

Then the first thing to do is to go to the hospital to check the physical condition of your husband and see if he has any diseases.

Generally speaking, there are two types of deaf-mutes: one is congenital deaf-mute and the other is acquired deaf-mute.

There are two more types of congenital deafness: one is caused by environmental factors such as X-ray exposure, viral infections, and teratogenic drugs in the early stages of pregnancy, and this deafness is usually not inherited. The other is hereditary, generally belonging to autosomal recessive inheritance, and there are also dominant inheritance, and there are three ways of inheritance:

1. The phenotype of the parents is normal, but they both carry the deaf-mute pathogenic gene, and the deaf-mute genes of the parents are passed on to the next generation, and a deaf-mute child will be born. If one of the parents is a carrier of the deaf-mute gene and is not deaf-mute, the next generation may also be a carrier of the deaf-mute gene and is not deaf-mute. 2. Both parents are born with hereditary deafness, and the children born are all deaf and mute, regardless of gender.

In this case, fertility is not allowed. 3. One of the parents is born with hereditary deafness, and among the children born, one-half may be a sick child, and one-half may be a normal child, which is calculated according to the law of heredity.

Acquired deafness and mute are caused by various external factors such as infectious diseases and drugs after the birth of the baby, and are not inherited.