Both parents have genetic diseases, should they have children?

The Marriage Act prohibits marriage for illnesses that are medically considered non-marriageable, including serious genetic diseases, designated infectious diseases, and related mental illnesses. Severe genetic diseases refer to genetic diseases caused by genetic factors, in which patients lose all or part of their ability to live independently, and their offspring are at high reproductive risk, and are medically considered unsuitable for childbearing. Both parties have severe mental retardation and are strictly forbidden to marry.

They can marry if they have other genetic diseases and do not have children after using long-term contraception or sterilization with the consent of both men and women.

In life, it is especially important for people to pay attention to eugenics. Having a healthy child is an expectation for the whole family, and those families who already know that they are sick and pass it on to the next generation will naturally be very cautious about having children. From a medical point of view, if the genetic disease is not a very serious type, then the child can reproduce in some way.

IVF, which is more technologically mature, can prevent children from inheriting disease genes by screening for high-quality genes, thus avoiding the transmission of diseases to children.

Couples who know they are sick should not have children because they can't even give the child a little bit of health. The children are cruel. Don't let the kids get bogged down.

Children cannot choose their own birth. If they still come into this world with illness, they will not only have to endure physical pain and suffering, but also the pressure of discrimination from others, their own psychological inferiority, and other negative emotions. It's really not fair to the kids.

Parents with children at home should know how difficult it is to raise children. Especially when a child suffers from a certain disease from an early age, they are not only physically and mentally exhausted, but also watching the child get sick and not being able to do anything about it. If you know in advance that your family has a genetic history, even if there is a 1% chance of affecting your child, you should think carefully.

Don't blindly inherit the family tree because of your own selfish desires, because you know you can't have healthy children. Otherwise, it will hurt the next generation.

Whether patients with genetic diseases can have children needs to be determined according to the actual situation, and receive formal genetic testing and evaluation before pregnancy, most patients with genetic diseases can conceive offspring through third-generation IVF technology or prenatal diagnosis and other measures, but there are also some hereditary diseases that cannot give birth to healthy offspring, such as the source Roche translocation, etc., it is recommended that such patients receive strict genetic disease testing before pregnancy; There are also some patients who are able and likely to have children, but given the severity of the disease.

If both parents have genetic diseases, then the child will definitely have a genetic disease, which is very unfair to the child and will also increase the burden on you.

If there is a genetic disease between the husband and wife, it will affect the fetus at this time, and the child will also have some genetic diseases.

You should not have children, because both parents have a genetic disease, so it is likely to be passed on to the child, so don't risk it.

In the face of such a situation, it is better for two people not to have children, because this is likely to lead to genetic diseases in the child.

Husbands and wives suffering from the same genetic disease should be forbidden to have children. If one of the parties suffers from one of the autosomal dominant diseases, X-linked dominant diseases, or polygenic diseases, they should also prohibit childbearing, so as to avoid the bad phenomenon of children.

Both parents have chromosomal dominant inheritance, linkage dominant inheritance, polygenic genetic diseases, congenital deafness, and these diseases are infertile, which will be passed on to their children.

It is not suitable for both parents to have linked recessive genetic diseases, chromosomal diseases, autosomal recessive diseases, polygenic genetic diseases, linked dominant genetic diseases, etc.

There are two types of epilepsy: primary and secondary. Primary epilepsy is a form of epilepsy caused by genetic factors, and the incidence of primary epilepsy is higher in relatives who are related to each other by blood, and vice versa. However, epilepsy is not entirely a genetic disease, but has certain genetic factors.

The most common types of epilepsy are acquired, such as cerebral hypoxia, encephalitis, traumatic brain injury, etc., which may cause persistent onset but are not inherited. Most of them can have children if the disease is well controlled.

Good attitude: Women should avoid emotional ups and downs during pregnancy and keep their mood comfortable, and women with epilepsy should pay attention to their own emotional regulation, so as not to affect the fetus in the womb and establish a healthy growth environment for the baby. Epilepsy can be divided into two categories: primary and secondary.

The originator** is still unknown; Secondary disorders may be caused by cerebral disorders (eg, cerebral vasospasm, encephalitis, meningitis, brain parasites, brain tumors). The secondary patients grasped the above primary diseases, and after a period of time, the condition improved steadily.

More than 500 genes have been found to be explicitly associated with epilepsy, and monogenic epilepsy refers to mutations in a single gene that cause seizures, including typical encephalopathy, febrile seizures, epilepsy caused by metabolic abnormalities, and brain or nervous system abnormalities. Studies have shown that most scholars believe that epilepsy is hereditary. According to statistics, the prevalence of the general population is about.

The prevalence of epilepsy in relatives of patients with primary epilepsy is two to six percent, which is 4 times higher than the prevalence of epilepsy in the general population, and I should say that it is hereditary! It doesn't matter if it's born or acquired: it's inherited!

It's just whether you can avoid the triggers the day after tomorrow: such as whether life is going well, whether there are setbacks, whether you encounter emergencies that people can't bear...And so on and so forth!!

More than 500 genes have been found to be explicitly associated with epilepsy, and monogenic epilepsy refers to mutations in a single gene that cause seizures, including typical encephalopathy, febrile seizures, epilepsy caused by metabolic abnormalities, and brain or nervous system abnormalities. Studies have shown that most scholars believe that epilepsy is hereditary. According to statistics, the prevalence of the general population is about.

The prevalence of epilepsy in relatives of patients with primary epilepsy is two to six percent, which is 4 times higher than the prevalence of epilepsy in the general population, and I should say that it is hereditary! It doesn't matter if it's born or acquired: it's inherited!

It's just whether you can avoid the triggers the day after tomorrow: such as whether life is going well, whether there are setbacks, whether you encounter emergencies that people can't bear...And so on and so forth!!

Epilepsy has a certain genetic predisposition. If both parents have epilepsy and you are also an epilepsy patient, it is important to have a doctor do a genetic evaluation before giving birth. Of course, the probability of a close marriage and a couple with epilepsy is still very low.

There are some dominant genetic diseases, serious recessive genetic diseases, polygenic genetic diseases, such as congenital mental illness, primary epilepsy, hepatitis B, retinocytoma, myotonic dystrophy, ascites and other genetic diseases, which are unable to have children.

Marfan syndrome, achondroplasia, hemophilia, myotonic muscle, Wilson's disease.

I think it is not appropriate for a husband and wife to have children when they are suffering from a very serious infectious genetic disease.

Chronic diseases, this condition is not suitable for childbearing, because this condition is also more dangerous, so once you have a child, you will inherit it to your child.

Polygenic genetic diseases, genetic diseases with more than two genes, chromosomal genetic diseases, and X-linked dominant genetic diseases are not allowed to have children.

Chromosomal diseases, linkage dominant diseases, polygenic genetic diseases, heart diseases, and psychiatric diseases, which are best not to have children, will bring serious harm to the body and cause problems in children.

Whether genetic diseases will affect fertility, it needs to be determined by the position of the pathogenic gene on the chromosome, and the genetic disease has a probability of being passed on to the child, but it is not 100%, please go to the hospital for a formal prenatal examination for the specific situation.

Genetic disorders are genetic diseases carried on human chromosomes, usually most of which are located on 22 pairs of autosomes, and a small number on sex chromosomes, but diseases located on the X or Y chromosomes are relatively more pathogenic to newborns.

In general, genetic disorders can be divided into two main categories: autosomal inherited diseases and incidental genetic diseases. Autosomal genetic diseases are divided into two types: autosomal dominant and autosomal recessive diseases, and there are x-dominant or recessive diseases and y-inherited diseases.

Sons born to patients with a genetic disease with Y are usually born, while daughters are not affected and have the same symptoms as their fathers. Typical diseases with Y heredity include long ear hair and webbed toes.

If the disease with X is dominant, the newborn will be affected by the presence of the disease-causing gene, regardless of whether the newborn is a boy or a girl. If you have a daughter with X recessive genetic disease, you need both X chromosomes of the daughter to carry the disease-causing gene to get sick, and only one of them will not be diseased, but if the newborn is a boy, as long as the X chromosome has a pathogenic gene, it will cause the disease, so there are far more men than women with such genetic diseases, especially the probability of disease will be greatly increased by the offspring of close relatives. The most typical type of recessive disease with X is hemophilia.

The salient feature of autosomal dominant diseases is that as long as there is one patient in the parents, the newborn is more likely to be affected by both males and females, and the probability of prevalence is equal for both males and females. Autosomal recessive disorders are caused by the presence of recessive pathogenic genes on autosomes, and the prevalence of consanguineous marriage is usually high, and the incidence of the disease is equal for men and women.

Marriage between close relatives is not only unethical and moral, but also increases the risk of illness for offspring, and parents should fulfill their corresponding responsibilities and not let their offspring suffer from undeserved diseases at birth because of their own impulses.

If you or your spouse have a corresponding genetic disease or carry a disease-causing gene, please do not rush to have offspring, you should learn to judge what gene causes the disease, if you can't make an accurate judgment, don't worry, go to a regular hospital and hand it over to a professional to solve.

It will not affect fertility, but it may be passed on to children, after all, it is a genetic problem, and there must be genes to be passed on to the next generation.

It does not affect fertility, but it is possible to be inherited. Heredity comes from the DNA of the parents, and the gene is the first to DNA, so genetic diseases can lead to inheritance.

It may affect their fertility function, depending on where the disease-causing gene is located on the chromosome. There is a certain probability of inheritance to children.