Diagnosis and Management of Intrauterine Growth Restriction and Congenital Anomalies
Trial Parameters
Brief Summary
The purpose of this prospective cohort study is to build a large platform that includes clinical information (prenatal diagnosis and postnatal follow-up data) and biological specimen banks of fetuses/infants with IUGR or congenital anomalies, which provide vital support and research foundation for accurate diagnosis, precision treatment and meticulous management.
Eligibility Criteria
Inclusion Criteria: All pregnant women who present to Guangzhou Women and Children's Medical Center meeting one of the following prenatal diagnoses and neonates/infants who are diagnosed as one of the following anomalies will be invited to participate: 1. Intrauterine growth restriction (IUGR) 2. Structural anomaly 3. Chromosomal anomaly Exclusion Criteria: 1. Pregnant women who don't agree to participate; 2. Pregnant women delivering babies at other hospitals. 3. Prenatally suspected anomalies that are not confirmed by postnatal diagnosis.