The importance of discovering genetic diseases in the early stages!

One of the biggest risks to fetuses is the genetic diseases that can affect it. Because their parents carry the gene gene, or that they themselves have the disease. Therefore, the couple before pregnancy or immediately after it occurred, the genetic tests. These tests are designed to reveal whether they carry the gene that the fetus could endanger. Three percent of children born annually carry genetic diseases or are born with a genetic defect. Often a child is born with a defect without his parents knowing that they themselves carry the gene that caused the disease. These people are completely healthy and carry the gene without developing the disease. Therefore, the genetic tests are performed to detect and reveal those who carry the gene or the risk that the child also carries. Only fifty percent of men choose to undergo genetic tests. This is although genetic diseases can be detected three times more than the past this day. Not performing the test threatens the fetus. However, if the test is done during the pregnancy planning period, the couple can decide whether or not they want a child. If the test is performed during pregnancy, a diagnosis of the condition of the fetus can be taken and a decision to proceed. Genetic tests are blood tests that are usually performed for the couple. There are groups that are more likely to develop genetic diseases, groups of people who fall within the marriage of family members, the couple with a family history of genetic diseases, or if another child has a genetic gene. If the parents have a genetic disease, they should not just take the test in the first pregnancy, even if they have a healthy child. However, if they have no genetic disease, it is not necessary to test in the second pregnancy. The possibility that parents will cause their children a genetic disease that is twenty percent. If it becomes clear that the parents have a genetic disease, the Placenta household foam test should be performed after the tenth week or the amniocentees after the sixteenth week. These tests diagnose the condition of the fetus. One of the most dangerous genetic diseases is Tai Zaks disease. This disease is transmitted to the fetus when both parents carry the disease -no. This disease occurs as a result of a lack of enzyme A, leading to the child suffering from mental disability, causing his death at the age of five. Tai Zaks is a serious but very rare disease. It belongs to 11 genetic diseases that are not curable. These diseases are fragile X syndrome, cystic fibrosis, canaban, Vanconony, Bloom, Dysautunomia Family Anti-Family Dysautonomia, Treasure Significant Herope, Mucolipidosis, Alpha-1 Anti-Tropene, Gaucher and Neimann Pick. Today, a simple blood test can be used to detect Tai Zaks disease, as well as other tests mentioned in the list above.