How to Detect Genetic Diseases Early in Pregnancy – A Simple Blood Test is Enough

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Forming a family needs a lot, even more than what you have expected. But, among all these things, what is more important than anything else is a healthy baby free from the possibility of genetic disorders and genetic diseases that may result in big problems and even in chronic health complications. A simple blood test can detect genetic diseases early in pregnancy and help you in ensuring good health of your kid.

There is no denying the fact that single-gene disorders are more common than Down’s Syndrome that need proper treatment and care. There is a safe prenatal test to help prospective parents decide what to do.

This is a wonderful test for genetic disorders that help women to learn about the future health of their baby as early as one to two months into pregnancy. This test would enable parents (intended couples and prospective parents) to choose whether to proceed with a pregnancy – if conditions like Huntington’s diseases and muscular dystrophy are detected.

Prenatal Diagnosis – Essential for Inherited Diseases

According to healthcare experts and doctors who are specialist in prenatal diagnosis, many inherited diseases like cystic fibrosis, hemophilia and sickle cell anemia can take place due to mutations within a single gene. According to them, there are more than 10000 single-gene conditions that can affect births. In that case, options for parents are very limited. However, pre-implantation genetic diagnosis can be used for the screening of embryos – mainly when couples are opting for IVF. For those who are planning pregnancy in natural way, amniocentesis test is important. It is important to note; such tests can carry small risk of miscarriage – but detect different genetic disorders.

However, another important part is that improvement can be seen in the speed and ease of safer test. Not to mention non-invasive prenatal test for Down’s syndrome that is done to detect single-gene diseases. This test is ideal to detect any single-gene disorder in the first 6 to 10 weeks of pregnancy. Such tests are done on the basis of DNA that looks for increases in the mutation level with a particular condition in the mother’s blood once she is pregnant.

Recombine’s CarrierMap Screening – A Revolutionary Test to Help Parents in Forming a Family with Healthy Child

Among different types of genetic screening test that are ideal for those who are early in pregnancy, planning a pregnancy or receiving fertility treatment. Such tests are also ideal for interested in their carrier status.

Recombine’s CarrierMap screening is one of the successful and advanced screening of genetic Carrier that brings a gamut of benefits. Being one of the most comprehensive and precise genetic carrier screen for individuals of all ethnic backgrounds, Recombine’s CarrierMap screening is ideal for those who are planning a pregnancy or currently expecting. This test is done to help them learning which mutation is present in DNA and how they could affect the health of your children.

This successful test for genetic screening is a miracle in medical world that has been helping thousands of parents to know about the risk of genetic disorders and then take the right treatment for ensuring overall good health of their baby. It helps parents and doctors to learn which mutations are present in your DNA and how they could affect the health. This successful test help in screening as much as 300 genetic conditions in just one blood sample. It can help you identify the chances of passing these genetic disorders to your child.

For this test, you need to reach the right center for a simple blood test.

Summary: There are different types of genetic screening tests like Recombine’s CarrierMap Screening is done to know about the risk of genetic disorders and how the affect can the baby in womb. You have to find the right clinic or center where such tests are done.

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