Fetal growth, development and genetics
Fetal anomalies, Fetal brain, Fetal growth restriction
Research aim
Our mission is to study normal and abnormal fetal development by innovative imaging modalities and (non)invasive genetic testing in order to improve perinatal and long-term outcomes of children and outcomes that matter most to future parents.
About us
We focus on early diagnosis of fetal anomalies and pregnancy outcomes using innovative ultrasound and MRI techniques, as well as advanced genetic testing. Our team has a special interest and expertise in the brain development in fetuses with different congenital anomalies including cardiac, gastrointestinal, and neurodevelopmental (both structural as acquired) anomalies as well as fetal growth restriction. We are specialized in assessing fetal development from the early first-trimester of pregnancy. We strive to optimize antenatal care for both mother and her unborn child, to reduce morbidity and enhance long-term quality of life.
Our multidisciplinary team is involved in prenatal counseling, guidance of the pregnancy and birth, and long-term follow up, all within a life cycle framework. Our multidisciplinary research team consists of fetal medicine specialists, neonatologists, fetal cardiologists, pediatric surgeons, fetal (neuro)radiologists, geneticists, ethical experts, who all work closely together with clinical geneticists and laboratory specialists. Moreover, our approach centers on patient values, prioritizing outcomes that resonate with our patients and their families. This is accomplished through the integration of patient-reported outcomes and the adoption of a life-cycle approach in our research endeavors. Our key partners therefore include patients and patient organizations. In addition, we closely collaborate with various (inter)national networks and partners.