At-home DNA test kits are prevalent everywhere. More and more people are opting for this test for their babies. Around 98% of new-borns undergo genetic screening in some form. Are these tests beneficial for the health of the baby, or they cause concern or worry?
In this article, we will learn more about the genetic testing process and its outcome.
What is the concern linked with at-home DNA test kits?
One of the major concerns linked to home DNA tests is that both doctors and parents can make false estimations of ailments based on the DNA findings of a newborn. These test kits are a nonspecific test for children that yields confusing information that would not prove beneficial for people.
The paternity test by PaternityUSA is performed by top-notch geneticists that use proven scientific methods to perform the highest quality testing at an affordable price.
What can a DNA test tell about a child?
A DNA paternity test is a wonderful medical procedure that can help identify specific nutrition genetic factors in a person. This includes gain in weight, loss in weight along with fibre and protein, predisposed vitamin deficiencies, salt consumption, blood pressure response, gluten sensitivity, and more.
The DNA-based nutrition report also assists in customizing the food requirement of the child so that he stays disease-free and healthy. By learning the child’s report of home paternity test, a parent will know how to inculcate good habits of eating vitamin boosting foods and certain fruits for maintaining their levels.
How Do At-Home DNA Tests Benefit A Child?
The home paternity test identifies a genetic mutation that is known to cause sensitivity towards a common antibiotic named gentamicin. Early diagnosis of the mutation and avoiding gentamicin could result in the prevention of chronic side effects, such as hearing loss.
Some physician-approved and consumer-initiated tests perform the test for over 190 childhood conditions that could be easily treated with dietary modification, medication, or another form of therapy. An example of such conditions includes anaemia, spinal muscular atrophy, atypical epilepsy, glycogen storage ailment, and specific childhood cancers.
Early detection of these conditions can help paediatricians and parents to take proactive steps in regards to the health of the child. You can stop the ailment by taking proactive steps and can easily prevent any potentially debilitating and non-reversible symptoms before their occurrence.
It provides a good analysis to parents regarding the response of the child to specific kinds of medications. This analysis includes identifying the response of the child to medications that are generally prescribed in childhood.
This analysis assists doctors to offer personalized treatment for the child throughout their life. In this way, it can help parents find whether their child will experience sensitivity or side effects to over 40 medications, including antibiotics.
Another important benefit of carrying out this test is that it gives mental peace to people. The simple summary chart tells what kind of medicines needs to be avoided based on the genetic variants the parent carries.
A DNA test/genetic test analysis helps parents find whether their child will experience sensitivity or side effects with medications, especially antibiotics. Thus, the outcome of this test assists doctors in offering personalized treatment for the child throughout life.