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Everyone knows that if parents have congenital genetic diseases, or do not do a good job of prenatal examination after pregnancy, it is very likely that the child will be found to have some congenital diseases after delivery. In fact, the birth of a child with a congenital defect is closely related to the physical condition of the pregnant woman and whether the pregnancy test is in place during the pregnancy test. <>
Pregnant women who give birth to a child with a birth defect also have the opportunity to give birth to a healthy child later in life. Some babies have congenital diseases, which have different reasons, some may be caused by genetic factors of parents, and some are caused by pregnant women who may have used some contraindicated drugs during pregnancy when they are pregnant, and the child is a congenital disease, so the prenatal examination during pregnancy is very important, and it is necessary to strictly follow the requirements of regular hospitals to do prenatal examination on time to reduce the probability of congenital diseases and malformations of infants. <>
Some congenital disorders, even if they are discovered after childbirth, can be**. Nowadays, science is so developed, there are many diseases that could not be overcome in medical treatment, and now they can be overcome, so even if the child has a congenital disease, it is necessary to go to some regular hospitals to check the child, and try to make the child heal, rather than letting it develop, because some diseases will be better when they are younger. <>
Parents should also not abandon a child if it is found that he or she has a congenital disease after birth. Children are innocent, every child wants to be healthy, with the love of parents, but some parents will discard their children when they find out that their children have congenital diseases, this practice is very chilling, whether it is morally or legally, this kind of behavior is not allowed, so when this situation occurs, we must think clearly, otherwise we will commit the crime of abandonment, not only condemned in conscience, but also punished in law.
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It depends on the genes of the parents, and if the doctor judges that they can have a healthy child, it is completely possible, after all, the technology is so advanced that it can also be tested after pregnancy. Bioimmune, cytogenetic and molecular genetic testing for the screening and diagnosis of hereditary diseases can help couples with adverse maternal history and infertility analysis**, and reduce the incidence of genetic birth defects.
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A: Yes. I think that the first child should be an accident, and the birth of the first child will not affect the birth of the second child, so you can still give birth to a healthy child.
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Yes, the first child is born with deafness, and it should have inherited the mutated gene of the couple, so it can be checked before pregnancy, and it is often encountered during pregnancy to ensure the health of the child.
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The first child suffers from congenital deafness, and the chance of giving birth to a healthy child is not large, generally this is a family genetic history, since the first child is disabled, in this case, it is better to go to the hospital to check and ask the doctor to see how much the chance of having a second child is healthy, and then decide whether to give birth.
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Yes, because congenital deafness is not a genetic problem of the parents, but the baby's own physiological defects, so if you have a second child, there is a high probability that you will not be deaf.
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Yes, deafness like this is also caused by genes or the environment in which it was raised, so there is a large component of the child's health.
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It is still possible to give birth to a healthy child, and congenital deafness may be caused by a genetic mutation, or by inattention during pregnancy.
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It is still possible to give birth to a child in a healthy manner, but it must be checked whether there is a family hereditary disease? This is important.
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It is possible to give birth to a healthy child. Whether the cause of a child's illness is genetic or a genetic mutation, it will have a certain impact on the next child, but it is not that a healthy child cannot be born.
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The chance is very small, don't worry, if you have the conditions, you can do some special tests such as chromosome tests, which can rule out some diseases, but they are expensive, and in addition, prenatal tests are also available now.
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Congenital deafness is related to the genes of the parents, and if the first child gives birth to a child with a disease, the next child will also have the probability of developing the disease, but it is not possible to specifically determine whether it is or not.
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This brings us to the recessive inheritance of hereditary deafness and de novo mutations. Most of the nonsyndromic deafness is autosomal recessive, if the parents each carry a disease-causing deafness gene, they themselves are only carriers and do not develop the disease, but there is a 25% probability that both disease-causing genes will be passed on to the child, and the child will suffer from hereditary deafness. Another rare situation is that during the development of the embryo, new mutations in genes caused by viral infections and environmental toxic factors lead to deafness.
There is currently no effective method of drug **. Wearing hearing aids or cochlear implants is an effective method.
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It is possible that congenital deafness is advisable, and it is recommended to have a timely hospital examination and**.
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There are genetic factors, and it is recommended to do a prenatal genetic test for deafness.
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The reasons are complex. It is possible that when I was in my stomach, I heard too loud noises. It could also be that the mother took inappropriate drugs.
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1.Genetic relationships. 2.Drugs cause relationships. 3.Causal disease.
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It is the child's deafness caused by abnormalities or genetic factors during the mother's pregnancy and childbirth, and it is mostly sensorineural deafness. Congenital deafness can be divided into two categories: hereditary and non-hereditary.
1.Hereditary factors.
Parents are born deaf, and children are susceptible to this disease. But not all of the children born are deaf. Second, consanguineous marriage can also cause congenital deafness. In addition, fetal ear tissue development malformations can also cause congenital deafness, but it can be corrected by surgery to restore hearing.
2.Drug intoxication.
During pregnancy, the mother used ototoxic drugs such as gentamicin and quinine, which can be carried through the placenta to the fetus, resulting in fetal seventh cranial nerve poisoning and deafness. If the mother has been deeply anesthetized during pregnancy, it can also cause hearing damage to the fetus.
3.Disease damage.
If one parent has a sexually transmitted disease, such as gonorrhea and syphilis, it can induce congenital deafness. The mother suffers from rubella and toxoplasmosis infection within three months of pregnancy, and the virus can cross the placenta and pose a threat to the fetus, causing malformations of inner ear development and deafness. Deafness can occur in newborns weighing less than 1,500 grams, suffering from hyperbilirubinemia, severe asphyxia during childbirth, and having purulent meningitis.
4.The process of childbirth.
When the mother is in labor, improper use of forceps can damage the child's hearing organs.
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Children are born with hearing loss, which can be caused by congenital causes. Most of them are due to genetic factors or the mother's viral infection such as rubella, measles, herpes, syphilis and the use of aminoglycoside antibiotics (streptomycin, gentamicin, kanamycin, etc.), or the mother's alcohol and drug abuse during pregnancy, which causes damage to the fetus's inner ear and auditory nerve. In addition, during the 4th to 28th week of pregnancy, when the fetal nervous system is developing, sudden noises or incorrect use of prenatal education** (more than 60 decibels) can affect the development of the fetal auditory nerve.
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This problem does not mean that adults have no problems, children have no other problems, deafness may be caused by poor growth during pregnancy, so now that pregnancy needs to be done, it is to see how the child develops and whether there is a disability.
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There is nothing wrong with the parents' hearing, and the child is born deaf. There are many reasons for this, what medicine may have been taken during pregnancy? It is also possible that the inheritance is several generations old, and so on and so forth, anyway, even if it is deaf, as long as the child is well trained, the child is still very promising.
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Deafness is not a genetic disease, this is often because the ears are not sound, this child is to put it bluntly, it is a little deformed, that is, the ears are not growing well!
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Congenital deafness, the inability to hear sound after birth, can occur on one or both sides, with varying degrees of severity. The main factors that contribute to congenital deafness include the following:
1. Parental genetics or inbreeding may affect children's hearing. Parents are born with deafness, and the child is susceptible to the disease. But not all of the children born are deaf.
Although some parents are not deaf, if they are close relatives, the incidence of deafness is higher. In addition, it is accompanied by auricular malformations, middle ear deformities, atresia of the external auditory canal, hypoplasia of the inner ear, or intellectual disability.
2. Maternal rubella or other viral infections during pregnancy: it may affect the hearing of the fetus. This is especially true when the mother suffers from the disease during the first trimester of pregnancy, when the fetus's hearing is more impaired. The virus can cross the placenta and invade the fetus, causing malformations of the inner ear.
3. The use of harmful drugs during pregnancy, such as quinine, streptomycin, gentamicin, etc., these ototoxic drugs circulate through the placenta, resulting in fetal seventh cranial nerve poisoning, thereby causing deafness.
4. The mother has been deeply anesthetized during pregnancy.
5. Ear tissue development malformation and insufficient birth weight of the fetus.
6. Parents suffering from sexually transmitted diseases, such as syphilis, can also cause fetal deafness.
7. Childbirth: premature birth or dystocia caused by hypoxia to the baby: or improper use of forceps damages the hearing organ and causes deafness.
Congenital deafness is not the same as hereditary deafness. Some non-inherited deafness in the inner ear is not passed on to the next generation.
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Congenital deafness refers to the development of hearing organs affected by various factors during the fetal period, which makes the auditory organs develop or are impaired, and the hearing impairment is pre-existing at birth.
Congenital deafness**.
1. Family history, consanguineous marriage, combined with congenital anomalies.
2. The mother has a viral infection in the first trimester of pregnancy, or has used aminoglycosides.
3. The newborn is a premature baby, hypoxic blood pressure or hyperbilirubinemia.
4. Fever in infancy.
Congenital deafness accounts for only 10 percent of the total number of deafnesses. Congenital deafness is not the same as hereditary deafness. Some non-inherited deafness in the inner ear is not passed on to the next generation.
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There are genetic factors, but other problems cannot be ruled out, some people are auditory nerve dysplasia during pregnancy, and there is a drug used during pregnancy that is not changed, if you are not at ease, you can go to the hospital for a genetic test.
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Not necessarily, if the meridians are cleared, there will be no deafness.
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Not necessarily, there are many possibilities, it depends on the actual situation.
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Because now society is full of poison. Food is poisonous, water is poisonous, air is poisonous, and the human heart is full of cancer. Adults don't know how much poison has accumulated in their bodies, and it is normal to pass it on to children.
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