Similar Questions with Answers
Question: Y double marker test needed?
Answer: The double marker test is a specific type of blood test with the goal to check for any anomalies that might be present in the chromosomal development of the baby. Having any abnormalities in the chromosomes can lead to serious health conditions, disorders, and so on that can affect the baby’s growth within the foetus, or even later in life. By knowing if there are any and checking for the right chromosomes that could be the issue, one can know beforehand about the presence or possibilities of certain disorders like Down’s syndrome, Edward’s syndrome and so on.
Question: Why double marker test needed?
Answer: Hello dear. Double marker test is screening blood test in pregnancy. ... So after an NT scan, after which you measure the amount of fluid at the back of the neck of the fetus and with the results, this double marker blood test is done and both the combined, and given a combined result as screen positive or negative. It is usually done after 8 weeks of pregnancy up to 14 weeks.
Question: is double marker test really needed?
Answer: Yes it helps to identify genetic chromosomal abnormalities in babies....