Explanation and Recommendations for Down Syndrome Screening Results

Interpreting the results of a high-risk Down syndrome screening and recommendations for whether to undergo amniocentesis

If a Down syndrome screening shows a 21-Three Body risk of one in ten, does it require further examination?

The baby has a broken palm on both hands, and the risk of Down syndrome screening during pregnancy was high. The low-risk result of non-invasive DNA testing suggests that the baby is unlikely to have Down syndrome.

Parents’ Concerns About Their Baby’s Growth and Development

This article explains the results and related questions about the Down Syndrome prenatal screening report, and provides some suggestions and answers.

The Down Syndrome screening result shows a high risk, and further amniocentesis and fetal chromosome testing are required to confirm the presence of Down syndrome.

Down Syndrome screening primarily targets children with congenital mental retardation, and if the test results show a risk exceeding the predetermined standard, further amniocentesis may be required to obtain more accurate results.

Down syndrome screening is a method of detecting potential Down syndrome in fetuses by measuring the levels of alpha-fetoprotein and human chorionic gonadotropin in the pregnant woman’s serum, and combining this with indicators such as gestational age, age, weight, and weeks of pregnancy to calculate the risk coefficient for having a child with Down syndrome.

Discussing the possibility of treatment for Down syndrome, as well as support and suggestions for patients and their families.