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The probability of chromosomal abnormality in three generations of test tube, the probability of gene mutation in three generations of test tube should be different from person to person. In short, three generations of test tube chromosomal abnormality probability is high or not this is really not good to say, mainly with their own choice is the hospital is not formal relationship, so in order to avoid doing three generations of test tube screening embryos after the occurrence of chromosomal abnormality, it is better to choose a formal, better technology test tube hospital to do three generations of test tube is better.

Three-generation test tube than a second generation of test tube more than one embryo before the transfer of genetic diagnosis, so in the embryo chromosome screening, can be no chromosomal abnormality of the embryo implanted in the body of a woman, so the probability of chromosomal abnormality of the three-generation test tube is in fact very small, however, because everyone's situation is not the same, some individual factors can still lead to chromosomal abnormalities in the three-generation chromosome, so chromosomal abnormality probability can not be The probability of chromosomal abnormality cannot be generalized.

The probability of chromosomal abnormality in three generations of test tube is high or not

The probability of chromosomal abnormality in three generations of test tube is high or not but also varies from person to person, although the three generations of test tube will be more detailed than the first and second generation of test tube screening, there are problems with the chromosome will generally be eliminated, but the three generations of test tube even after the screening of chromosomal abnormality may occur, because there are a lot of factors leading to chromosomal abnormality, and the specific situation of each person is also different. So the probability of causing chromosomal abnormalities in three-generation test tube is also different.

The probability of chromosomal abnormality in three-generation IVF is actually very clear. Doing three-generation IVF can detect 95% of chromosomal problems, so the probability of chromosomal abnormality is also lower than that of the first and second generation of IVF. However, three-generation IVF cannot guarantee 100% screening of abnormal chromosomes, and the bad qualification of the hospitals, the imprecise screening technology, and improper operation of the laboratory personnel may all affect the probability of chromosomal abnormality.

Probability of genetic mutation after three-generation IVF screening

The purpose of three-generation IVF is to prevent chromosomal abnormalities from being passed on to the next generation and to achieve eugenics, so the probability of genetic mutation after three-generation IVF screening is very low, and after three-generation IVF screening, the majority of babies born will not have a genetic mutation, but three-generation IVF is only able to screen hundreds of genetic diseases, and it is not guaranteed to screening for new genetic diseases.

Under normal circumstances, three generations of test tube on the embryo after screening is not going to inherit chromosomal abnormalities and genetic diseases to the child, so the probability of three generations of test tube gene mutation is not as high as imagined, three generations of test tube can be screened for genetic diseases and chromosomal abnormalities in the following areas.

1, third-generation test tube testing chromosomes, check whether the number or structure of chromosomes is abnormal, PGD technology is to detect genes, diagnose whether the embryo carries defective genes or genetic disease-causing genes, and then remove the defective embryos and select healthy blastocysts to be transplanted into a woman's uterus, which can avoid the birth of defective babies;

2, the third-generation test tube technology can accurately diagnose hemophilia, congenital deafness, colorblindness, thalassemia, spinal muscular atrophy and more than 200 kinds of genetic diseases, effectively avoiding the impact of these genetic diseases, avoiding the risk of genetic defects in newborns, and comprehensively protecting the health of infants;

3. Third-generation IVF technology can prevent the fetus from suffering from hereditary diseases, because the embryo will be tested before embryo transplantation, and through the testing of genes and chromosomes of the embryo, abnormal embryos will be removed if found to be abnormal, so that the fetus can be born free of hereditary diseases. diseases.

It can be seen that the probability of genetic mutation after three-generation IVF screening is really not high although it is not zero, but because each person's situation is different, three-generation IVF can not guarantee new genetic mutations and other genetic mutations that can not be screened, so the probability of genetic mutation is also different from person to person.

Three-generation test tube than a second generation of test tube more than one embryo transplantation to do a genetic diagnosis, so in the embryo chromosome will be screened, can be no chromosomal abnormality of the embryo implanted in the body of a woman, so the probability of chromosomal abnormalities three-generation test tube in fact, is very small, but because everyone's situation is not the same, some individual factors can still lead to chromosomal abnormalities in the three-generation, so chromosomal abnormality probability can not be The probability of chromosomal abnormality cannot be generalized.

The probability of chromosomal abnormality in three generations of IVF, genetic mutation is really not that evil is briefly introduced here. If you want to know more about IVF costs, IVF hospitals, IVF success rates and other related knowledge, you may want to consult the IVF channel on the preferred reproductive experts, one-on-one for you to answer.