Treatment Recommendations for Down Syndrome

The Down syndrome screening test shows a critical risk for trisomy 21, do I need to undergo a non-invasive DNA test?

If the Down syndrome test result indicates a high risk, it is recommended to undergo amniocentesis to confirm the baby’s condition.

Down Syndrome typically does not present with any noticeable symptoms during pregnancy and requires prenatal screening tests such as the Down syndrome test for detection. If the screening results indicate a higher risk, further tests like non-invasive prenatal DNA testing or amniocentesis may be needed to confirm any chromosomal abnormalities. If chromosomal abnormalities are confirmed, it may be necessary to consider terminating the pregnancy.

Although the Down syndrome screening is high-risk, if amniocentesis is not performed and the newborn screening is normal, how should one further confirm the condition?

Treatment and prevention methods for children with Down Syndrome, as well as suggestions for surgical correction.

If the Down Syndrome screening result is not passed, how should one proceed with further examinations?

If the Down Syndrome screening result is 1 in 44, how should you handle this situation?

If the Down Syndrome screening result is high-risk, how should one respond?

If a Down syndrome screening indicates high risk, how can one further determine the fetus’s health condition?