Being an aspected parent is an amazing feeling that every mother understands. During pregnancy, they need to be extra careful and require lots of testing procedures to consider in nine months. One such testing or screening is prenatal genetic testing.
Prenatal genetic testing is a powerful tool in modern medicine that allows aspected parents and healthcare professionals to access the developing status of a baby. This tasting can provide valuable information on the health and well-being of an upcoming baby. These insights can help parents to make informed decisions about their pregnancy and prepare for any potential medical concerns.
However, like any other medical procedure, prenatal testing has its own risks and benefits. So, let’s understand these factors while understanding the term prenatal genetic testing.
What Is Prenatal Genetic Testing?
Prenatal genetic screening is a group of diagnostic procedures that helps to identify the genetic abnormality of the developing fetus. These tests provide information about the baby’s genetic makeup that allows the health care provider to access certain genetic risks.
It is an optional procedure where parents can choose based on various factors. These factors may include the mother’s age, family history, and specific medical conditions. With this understanding, let’s proceed further and learn about the types of prenatal genetic testing before delving into the risk factors.
Types Of Prenatal Genetic Testing
The first and the most common test is the ultrasound, which is also important for the expected mother. It is the routine part of parental care and can provide valuable information about the baby’s development. They can reveal the abnormality of the fetus, such as heart defects or neural tube defects.
2] Non-Invasive Prenatal Testing (NIPT)
The second test is non-invasive prenatal testing or NIPT, which involves a sample of blood drawn from the mother and detecting a chromosomal abnormality. These abnormalities may include Down syndrome, trisomy 18, and trisomy 13. NIPT is considered one of the safest prenatal genetic testing and has a high accuracy rate.
3] Chronic Villus Sampling (CVS)
CVS is an invasive testing that involves small pieces of tissues from the placenta for genetic analysis. The test is typically performed between 10 and 13 weeks of pregnancy to detect chromosomal abnormalities and genetics. By grabbing this information, doctors can provide the necessary diagnostic procedures to provide a healthy birth.
The invasive procedure is amniocentesis, where a sample of amniotic fluid is collected. These elements are used to check the abnormality and genetic condition of a baby. This prenatal genetic test is performed between 15 and 20 weeks of pregnancy.
5] Carrier Screening
Last on the list is carrier screening, which helps to identify if either parent carries a gene for a specific genetic condition. These genes may include cystic fibrosis or sickle cell Armenia, which can be potentially transferred to the baby. If both parents carry the same gene, then the baby has a higher risk of inheriting the condition.
Risks And Factors To Consider During Prenatal Genetic Testing
1] False Positive And False Negative
No prenatal genetic testing can be 100% accurate, which can lead to unnecessary stress and invasive follow-up tests. False negatives may also provide false reassurance, which makes it crucial to understand the limitations of these tests.
2] Invasive Testing Risk
The second risk comes with procedures like CVS and amniocentesis, which may lead to the risk of miscarriage. The expected parents should weigh the benefits against the potential risks.
3] Emotional And Ethical Consideration
Prenatal genetic testing may reveal information that is emotionally challenging or ethical complexes. In such cases, the decision to continue the pregnancy can be difficult for both the father and mother.
4] Need For Genetic Counseling
Sometimes, prenatal testing results may lead to depression, which may affect the pregnancy phase. So, it is advisable to seek genetic counseling before and after testing to interpret the result, understand the implications, and make informed decisions.
Understanding The Baby Genetic Health
Other than the above factors, cost and time are the two elements that need to be considered to avoid any type of complications. Before going for prenatal genetic testing, take insurance coverage and be on time for certain tests. Also, take into account the unique circumstances and preferences under the guidance of the doctors or healthcare professionals.