NIPT – non-invasive prenatal test

Prenatal diagnostics – safety for mother and child, e.g. through Non-invasive prenatal testing (NIPT) from a maternal blood sample.

Prenatal diagnostics allows us to gain early information about your baby's development and identify potential risks. Using modern techniques such as ultrasound examinations and genetic testing, we can offer you precise and reliable diagnostics. Our goal is to provide you with peace of mind and clarity, allowing us to optimally support you throughout your pregnancy.

Non-invasive prenatal testing (NIPT) uses cell-free fetal DNA from a pregnant woman's blood sample to extract genetic information about the fetus—such as trisomy 13, 18, and 21. These tests carry no risk of miscarriage compared to invasive methods such as amniocentesis or chorionic villus sampling.

Amniocentesis

Amniocentesis may be indicated in cases of abnormal first trimester screening to assess the risk of genetic diseases.

Amniocentesis, also known as amniotic fluid testing, is a diagnostic method used in certain cases to detect genetic or chromosomal abnormalities. It can be performed starting from the 15th week of pregnancy and provides valuable information about your baby's health. As part of our care, we place great emphasis on comprehensive counseling and individualized risk assessment to support you in this important decision.