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Why to Determine Genetic Compatibility With Your Partner

The billions of tiny cells that make up the human body store information about its functionality. They make people alike and different at the same time. Each person has thousands of genetic variants in their DNA.
Accidental violations in DNA can be transmitted from generation to generation for a long time without any symptoms. However, they can manifest themselves in the form of infertility, pregnancy complications, and lead to the birth of a child with a hereditary disease at the most crucial moments of life when you met a perfect partner on snapsext. The reproductive system is controlled by about 2000 genes. Mutations in any of these genes, and sometimes a change in the structure of an entire chromosome, can lead to disruptions in the functioning of the reproductive organs, which can lead to infertility, or lead to the fact that a woman cannot bear and give birth to a healthy child.

Conception issues

Infertility and other diseases of the reproductive system can be caused by certain mutations in the human genome. It is about changes in the number and structure of chromosomes and mutations of individual DNA fragments. Usually, such disorders do not have any manifestations before planning a pregnancy, and both partners with such a genetic disorder consider themselves healthy.
Modern medicine is not yet able to correct genetic disorders, but a timely diagnosis of the causes allows you to solve the problem of infertility with the help of assisted reproductive technologies. They are effective when the exact cause of the reproductive disorder, including the genetic one, is established.

Complications during pregnancy

Genetic factors are one of the main causes of pregnancy complications, for example, it is about genetically determined predisposition to thrombophilia. Thromboses that occur during pregnancy in the vessels of the placenta can lead to obstetric pathology.
The revealed predisposition doesn’t suggest the presence of a disease, it indicates the likelihood of its development, which makes it possible to prevent the consequences of unfavorable genetic characteristics of the mother and to ensure the normal course of pregnancy. The doctor can adjust the prevention plan, prescribe additional tests, or make changes in the therapy based on the results of the genetic test.

Hereditary diseases of the child

One in fifty newborns has a genetic disorder or serious congenital malformation. More than 20% of child mortality is the result of abnormalities in the baby's DNA. Children with genetic diseases can be born to young healthy parents even if other family members do not have such diseases. If both parents are carriers of the same hereditary disease, then with a probability of 25%, their kid will be born with severe hereditary disease. Having one normal copy of the gene allows the body not to experience any problems.
Conducting a DNA test for the carriage of such mutations will make it possible to find out in which genes the mutations are located. Medicine cannot correct mutations in parents, but after their detection, it becomes possible to make some reproductive procedures that will significantly reduce the risk of having a sick child. To avoid problems at any stage of planning and childbirth, it is important to know about the possible genetic disorders of both partners.
Each person carries 2-5 pathogenic mutations responsible for the development of fatal hereditary diseases. If both parents carry a mutation in the same gene, the chance of having a sick child is 25%. To establish the causes of infertility, realize the risks of developing diseases during pregnancy, and reduce the likelihood of having a sick child, it is important to identify the possibility of hereditary disorders beforehand.

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