Yes, testing is possible, but there are a few important points to be aware of.
In cases of vanishing twin, the DNA of the twin who has stopped developing remains in the mother’s bloodstream for some time. As a result, there is a higher risk of inaccurate results (results that differ from the true condition) compared to a single pregnancy.
At our clinic, we may perform testing as an exception for patients who fully understand and consent in writing to this “risk of reduced test accuracy.” To help maximize accuracy, the test (blood draw) must be performed at or after 10 weeks of pregnancy.
If you have any concerns or questions, please do not hesitate to speak with our doctors or staff at your appointment.

Yes, accurate testing is performed under all plans. However, since the scope of testing differs by plan, please choose the one that best matches your goals.

These abnormalities can significantly affect a child’s development and health after birth. Knowing in advance allows families to prepare and seek appropriate support.

NIPT can screen for chromosomal abnormalities (such as trisomy 13, 18, and 21), sex chromosome abnormalities, whole-chromosome partial deletions and duplications, and microdeletion/duplication disorders.

Domestic testing is based on data from pregnant women in Japan, and covers conditions such as whole-chromosome partial deletions and duplications, as well as sex chromosome abnormalities.

A comprehensive plan allows you to gain a broad understanding of your baby’s health before birth, enabling early preparation and access to appropriate medical care when needed.